Background of The Invention Conventional surfactants have one hydrophilic group and one hydrophobic group. Dimeric surfactants which are commonly called "Gemini"surfactants are those which comprise two hydrophilic functional groups and two hydrophobic functional groups. Gemini surfactants have unique physical properties resulting from constraint of two hydrophilic groups in close proximity and the consequent micellar properties, which has led to an intensive study of Gemini surfactants as detergents, softeners, emulsifiers, phase transfer catalysts, biocides, and as components in skin care lotions, hair conditioning compositions and cosmetics compositions. Their use is also being investigated in ore flotation, oil well drilling and in other industrial applications.

It is therefore an object of the present invention to provide a novel class of cationic multiple functional surfactants that have application in the treatment of textile fibers to provide softeners and static control.

It is also an object to provide a class of multiple functional surfactants having improved detergency at extremely low concentrations, while at the same time being highly biodegradable.

It is also an object of the present invention to provide a class of multiple functional surfactants which are useful as emulsifiers, phase transfer catalysts, biocides, in ore flotation, in oil well drilling and in other related applications.

Finally, it is an object of the invention to provide a class of multiple functional surfactants which are useful in skin care lotions, hair conditioning compositions and cosmetics compositions at low concentrations.

These and other objectives are realized by the compositions and methods of the present invention.

Summary of the Invention The present invention generally relates to several new classes of cationic multiple functional surfactants and to compositions containing same. The invention also relates to various processes for preparing the multiple functional surfactants of the present invention.

Detailed Description of The Present Invention The present invention generally relates to multiple functional surfactants of the formulae I-IV, below, to compositions containing same and to methods for their preparation. The beneficial features of the multiple functional surfactants of the present invention derive from their multiple functional character, i. e., the chemical species of the present invention contain two or more hydrophobic groups and two or more hydrophilic groups in each molecule.

I. Multiple functional quaternary ammonium compounds containing ester or amide spacer group (s) of the general formula: wherein R, and R2 are the same or different and are selected from straight or branched chain, substituted or unsubstituted C,-C22 alkyl or alkenyl groups wherein said alkyl or alkenyl groups optionally contain at least one ester linkage, at least one amide linkage, or mixtures thereof; R3, R4, R5, and R6 are the same or different and are selected from straight or branched chain, substituted or unsubstituted C,-C22 alkyl or alkenyl groups wherein said alkyl or alkenyl groups optionally contain at least one ester linkage, at least one amide linkage, or mixtures thereof; and A is a spacer selected from the group consisting of: or other ester-or amide-functional alkyl groups in the spacer,

wherein each of x, y and z can independently be an integer of 1-20 ; and n is an integer of from 1-20; II. Multiple functional quaternary ammonium compounds with ester or amide spacer group (s) of the general formula: wherein R,, R8, R9, R10 R11, R12, R13, and R14 are the same or different and are selected from straight or branched chain, substituted or unsubstituted C,-C22 alkyl or alkenyl groups, wherein said alkyl or alkenyl groups optionally contain at least one ester linkage, at least one amide linkage, or mixtures thereof; and A is a spacer group as defined above, and wherein x, y and z are each independently an integer of 1-20; and n is an integer of from 1-20 : or 111. Asymmetric multiple functional quaternary ammonium compounds: wherein Rs and R20 are different and are selected from straight or branched chain, substituted or unsubstituted Cs-C22 alkyl or alkenyl groups wherein said alkyl or alkenyl groups optionally contain at least one ester linkage, at least one amide linkage, or mixtures thereof; R16, R17, R18

and Rig are the same or different and are selected from straight or branched chain, substituted or unsubstituted C,-C22 alkyl or alkenyl groups wherein said alkyl or alkenyl groups optionally contain at least one ester linkage, at least one amide linkage, or mixtures thereof : and n is an integer of from 1-20.

IV. Symmetric"gemini"quaternary ammonium compounds prepared in the reaction of alkyl multiple amine compounds with long chain aldehyde or alcools of the aeneral formula IV wherein R2,, R22, R23, R24, R25, R26, R2,, and R28 are the same or different and are selected from straight or branched chain, substituted, or unsubstituted C,-C22 alkyl or alkenyl groups, wherein said alkyl or alkenyl groups optionally contain at least one ester linkage, at least one amide linkage or mixtures thereof, and where x an y are each independently an integer of from 1-20 and n is an integer from 0-20 ; wherein in each of 1, II, III and IV, Z-is an anion.

In each offormutae NN, above, R"R2, R7, R, 4, R, s and R20 are preferably selected from C8-C18 alkyl groups, optionally containing an ester linkage. It is also preferred that x, y and z are 0-5 and that n is 1- 10.

In formula IV above R2, and R25 are preferably selected from 2- ethylhexyl. nonyl-alkyl, or a C13-C15 mixed alkyl group, and R22, R23, R24, RZS R26, R2-, and R28 independently selected from methyl, ethyl, or propyl, and n = 0, 1, or 2.

Concerning the multiple functional quaternary ammonium compounds of formula 1, it is preferred that R, and R2 be selected from 2- <BR> <BR> <BR> ethylhexyl, nonyl-alkyl, a C, 3-C1s mixed alkyl group, or from the group consisting of dodecylalkyl, hexadecylalkyl, octadecylalkyl, oleylalkyl, cocoalkyl, soyaalkyl, tallowalkyl, or hydrogenated tallowalkyl; that R3, R4, Rs and R6 be independently selected from methyl, ethyl, propyl, 2- <BR> <BR> <BR> ethylhexyl, nonyl-alkyl, or a C3-Cas mixed alkyl group; and that n be an integer of from 1 to 5.

In the multiple functional quaternary ammonium compounds of formula II, it is preferred that each of R,, R8, Rg, R, o, R"R, z, R, 3 and R, 4 are independently selected from from methyl, ethyl, propyl, 2-ethylhexyl, nonyl-alkyl, a C, 3-Crs mixed alkyl group, or from the group consisting of dodecylalkyl, hexadecylalkyl, octadecylalkyl, oleylalkyl, cocoalkyl, soyaalkyl, tallowalkyl, or hydrogenated tallowalky; and that n be an integer of from 1 to 5.

Finally, it is preferred that, in the asymmetrical multiple functional quaternary ammonium compounds of formula Ht, R, 5l R16, R17, R18, R19 , and R20 be selected from methyl, ethyl, propyl, 2-ethylhexyl, nonyl-alkyl, a C, 3-Cns mixed alkyl group, or from the group consisting of dodecylalkyl, hexadecylalkyl, octadecylalkyl, oleylalkyl, cocoalkyl, soyaalkyl, tallowalkyl, or hydrogenated tallowalky or other long chain fragment with the proviso that the group of substituents on one N'be not identical to the group of substituents which surround the other N'center and that n is an integer of from 1 to 20.

The ester or amide containing multiple functional compounds of the present invention exhibit enhanced biodegradability which is extremely desirable for obvious environmental reasons. For example, enhanced biodegradability is a desired attribute in fabric softening

compositions and in other uses where the content and volume of waste water effluent streams needs to be controlled.

When used in a fabric softening composition, the compounds of the present invention are preferably delivered to the textile to be softened in amounts effective to impart the desired softness and/or anti-static properties to said textile (s). Said effective amount typically ranges in an amount of from about 0.5 to 3 grams of softening compound (s) per average load of laundry.

Delivery of the compounds of the present invention to the textile to be treated can be conducted by various means. For example, the compounds of the present invention can be formuiated into liquid softening compositions, solid formulations and/or solid articles. In a liquid formulation, the compounds of the present invention are dissolved and/or suspended in water, wherein said formulation optionally also contains other conventional softeners as well as other ingredients and diluents such as detergents, optical brighteners, viscosity aids, soil release agents, fragrance, and the like, in the requisite amounts so to provide an effective amount of the compounds of the present invention to the textile to be treated.

With solid formulations, the multiple functional surfactants of the present invention are formed into small flowable particles or beads on a water-soluble carrier such as a solid detergent, which is optionally compounded with builders, brighteners, fragrance and the like.

Finally, the multiple functional surfactants of the present invention can be combined with a distribution agent and applied, or coated on a solid carrier such as a woven, or non-woven fabric or bonded polyester

sheet. Alternatively, the composition can be inserted into a container designed for insertion into a clothes dryer.

The present invention also relates to various methods for the preparation of multiple functional surfactants. For example, the multiple functional surfactants of formula I which contain ester spacer groups can be prepared by reacting a dialkylalkanol amine of formula wherein each of Q,, Q2 and Q3 is independently selected from the group consisting of C,-C22 alkyl groups and a dicarboxylic acid of the formula HOOC- (CH2) nCOOH wherein n is an integer of from 1-12, to form a reaction mixture, or a diester of same, and thereafter quaternizing the reaction mixture.

The dialkylalkanol amine is preferably prepared by ethoxylating a fatty amine compound of the formula Wherein Z is a C, 2-C22 substituted or unsubstituted, saturated or unsaturated, straight or branched chain alkyl group, and Y is a C,-C22 substituted or unsubstituted, saturated or unsaturated, straight or branched chain alkyl group.

Preferably, the fatty amine compound is selected from the group consisting of dodecylamine, hexadecylamine, octadecylamine, oleylamine, cocoalkylamine, soyaalkylamine, tallowalkylamine, hydrogenatedtallowalkyl amine, dicocoalkylamine, ditallowalkylamine, dihydrogenated tallowalkylamine, dioctadecylamine, and mixtures thereof.

The dicarboxylic acid employed is preferably selected from the group consisting of oxalic, malonic, succinic, glutaric, adipic, maleic, fumaric and

mixtures thereof. The most preferred dicarboxylic acid is adipic acid, or mixed short chain di-acids which are commercially available from, for example. DuPont.

The multiple functional surfactants of formula I which contain an amine-functional spacer group can be prepared in the reaction of an N- alkylamino fatty amine compound R-N (H) (CH2) NH2 with a dicarboxylic acid or mixtures of dicarboxylic acids (or diesters of same).

The multiple functional quaternary ammonium compounds of Formula IV can be prepared by reacting a bis-primary amine alkane (e. g., hexamethylenediamine) with two equivalents of aldehyde, e. g., 2- ethylhexanal, or other long chain aldehydes such as nonanal or mixed Cr3-Crs aldehydes (which are commercially available).

Other multiple functional quaternary ammonium surfactants of general Formula IV of the present invention can be prepared by reaction of aliphatic triamines of formula: wherein R is a saturated or unsaturated hydrocarbon group, with aldehyde, e. g., 2-ethylhexanal, or longer chain aldehyde such as nonanal or mixed C, 3-C, 5 aldehydes (which are commercially available), or an alcool. For example, tris-quaternary ammonium surfactants can be prepared by reaction of bis (hexamethylene) trimine with alkylaldehyde, such as 2-ethylhexanal, followed by methylation and quaternization.

The cationic gemini and related multiple functional hydrophilic/hydrophobic functional compounds of the present invention can be employed alone, or in combination with typical surfactants,

including mono-quaternary ammonium compounds. When employed in combination with mono-quaternary ammonium compounds, it has been found that as little as 5-10% of the compounds of the present invention can reduce the Critical Micelle Concentration (CMC) from 10 up to 100 fold. CMC is a measurement employed to determine the effectiveness of a surfactant composition. The lower the CMC values, the better the surfactant. Thus, by using small amounts of the surfactants of the present invention in combination with conventional surfactants, the addition rates of the conventional surfactants can be greatly reduced.

The present invention shall now be illustrated by the following non- limiting examples.

Example 1-Preparation of a Multiple Functional Quaternary Ammonium Compound with Ester-functional Spacer Groups Preparation of (_C02CH2CH2NMe2) 2 from adipic acid and dimethylethanolamine in toluene Procedure-A 1 L round bottom flask was charge with 14.6 g of adipic acid (1.00 mole), 196.0 g of dimethylethanolamine (2.20 mole-10% excess), 300 mL toluene and 1.5 g of p-toluenesulfonic acid. The reaction mixture was heated to reflux with stirring. A Dean-Stark trap was attached to one neck of the 4-neck flask and to a water condenser. The reaction was heated at reflux for a total of 22 hours as 54.5 mL H20 distille. The product was stripped of solvent on a rotary evaporator at 80° C and 15 mm Hg. The product weighed 270.6 g. Infrared spectroscopy of product indicated only the ester.

Reaction of (CH2) 1 (CO2CH2CH2NMe2) 2 with hexadecyl bromide

Procedure-A 1 L Morton flask was charged with 57.6 g of (CH2) 4 (CO2CH2CH2NMe2) 2 (0.2 mole) and 300 mL of monoglyme. 122.0 g <BR> <BR> <BR> C, 6H33Br (0.4 mole) were added with stirring. The mixture was heated to 85° C with stirring under an N2 atmosphere and maintained for 73 hours.

No solid was evident at the conclusion of heating but did form on standing over several days. The total product was suction filtered and the beige solid was sucked dry. It was then washed twice with diethylether and again sucked dry, then let stand in a crystallization dish overnight. The solid product weighed 135.5 g (theoretical yield: 179.6 g). Another 30.8 g solid product was reclaimed from the filtrate for an overall yield of 92.6%.

NMR analysis of product indicated 80 mole % purity of diquaternary compound, 14 mole % mono-quaternary and 6 mol % mono-quaternary- monoacid product.

A composition was prepared comprising 90% Arquad 12 (available from Akzo Nobel Chemicals Inc., Chicago, IL) and 10% of the compound of example 1. This composition exhibited a 50 fold reduction of CMC values compared to a composition comprising 100% Arquad 12.

Example 2-Preparation of Multiple Functional Quaternary Ammonium Compound in Reaction of Aldehyde with Alkyl-diamine: reaction of 1.6- hexanediamine with mixed C13/C, 5 aidehyde. followed by reduction. methylation, and quaternization Summary: H2N (CH2) 6NH2 + 2 RCHO o RCH=N (CH2) 6N=CHR sodium borohydride CH3 CH3 methylation RCH2N (CH2) 6NCH2R R RCH2NH (CH--1) 6NHCH2R CH3CI RCHO = C3-C15 aldehydc CH3 CH3 + RCH2N (CH2) 6NCH, R CH3 CH3 2Cr

1. Reaction of 1,6-hexanediamine with mixed C, 3/C, 5 aidehyde. The mixed aldehyde was used as obtained from Celanese Ltd.

Chemicals Division (Dallas, TX); the average molecular weight was estimated to be 211. The aldehyde mixture (400 g., 1.89 moles) was added in portions to melted 1,6-hexanediamine (107 g., 0.92 mole). The reaction was exothermic and was therefore cooled occasionally. The product was washed with water; after solvent was removed by evaporation, a oily yellow liquid (428 g.) was obtained.

2. Sodium borohydride (32 g.) was added as powder to a solution of the bis-imine compound (404 g., product in 1 above). The reduction reaction was followed by observing disappearance of the imine carbon's 13C NMR. The reaction mixture was washed thoroughly with water before solvent was removed by evaporation.

The product was a pale yellow liquid (400 g.) 3. Methylation of the bis-secondary-amine by Eschweiler-Clarke procedure (see also Leukhart Reaction, Organic Reactions, Volume 5, p. 323). To the bis-sec-amine (360 g., 0.71 mole) 90% formic acid was added slowly, forming a light brown solution as the reaction temperature increased to 75° C and then cooled to 50-60° C. The 37% formaldehyde (66 g., 0.814 mole) was slowly added as CO2 gas evolved. The mixture was heated until gas evolution ceased. Ca. 80 g. of concentrated HCI was added, and the formic acid and any excess formaldehyde were removed at 65° C on a rotary evaporator. The residue was dissolved in water and neutralized with 25% aqueous NaOH (ca. 65 g.). The product was washed with water and dried. A pale yellow liquid (440 g.) was obtained and identified as the bis-tertiary amine.

4. Quaternization of the bis-tertiary amine compound prepared in 3 above. In a 1-liter titanium autoclave, a solution of bis-tertiary- amine in methanol (150 g) with sodium bicarbonate was purged with nitrogen and heated with methyl chloride at about 80°C until all amine had been consumed (in about 10 hours). Filtration and evaporation yielded a brownish yellow thick paste (215 g.) that was identified as the bis-quaternary ammonium compound.

Example 3-Preparation of Asymmetric Multiple Functional Quaternarv Ammonium Surfactant Compounds Asymmetric dimeric-or higher oligomeric surfactant compounds are prepared from Duomeen@, Triameen0, and Tetrameen compounds available from Akzo Nobel Chemicals Inc., Chicago, IL, using an amine- aldehyde condensation reaction. H H H HH H H H ~/+ 2-ethylhexanal o o -"" + 2-ethythexana)--" " Duomeen where R = coco-, tallow-, or oleylaikyl H H I I R-NN-ethyhexyl + methylation, quaternization o CH3 CH3 R-NN ethyhexyl CH3 CH3 2Br- Example 4-Preparation of Multiple Functional Quaternary Ammonium Compound in the reaction of bis (hexamethylene) triamine with mixed C13/C15 aldehyde, followed by reduction. methylation. and quaternization

1. The mixed aldehydes were added in portions to melted bis (hexamethylene) triamine; and the exothermic reaction was cooled. The reaction mixture was washed with water, then solvent removed by evaporation to yield the bis-imine mono-secondary amine compound, a pale yellow liquid.

2. Reduction of the bis-imine-mono-sec-amine compound with sodium borohydride. The bis-imine compound (283 g.) prepared in 1 above was dissolved in 150 g. methanol. To this 25 g. sodium borohydride was added in small portions until the reduction was complete. The reduction reaction was followed by observing disappearance of the imine carbon's 13C NMR. The reaction mixture was washed thoroughly with water before solvent was removed by evaporation. The product was a pale yellow liquid (247 g.) 3. Methylation of the tris-secondary amine compound prepared in 2 above. The tris-sec-amine compound (245.6 g., 1.17 mole). To this solution, formic acid was added slowly, forming a light brown solution as the reaction temperature increased to 75° C and was then cooled to 50-60° C. The 37% formaldehyde (66 g., 0.814 mole) was slowly added as CO2 gas evolved. The mixture was heated until gas evolution ceased. Ca. 80 g. of concentrated HCI was added, and the formic acid and any excess formaldehyde were removed at 65° C on a rotary evaporator. The residue was dissolved in water and neutralized with 25% aqueous NaOH (ca.

65 g.). The product was washed with water and dried. A pale yellow liquid (247 g.) was obtained and identified as the tris-tertiary amine.

4. Quaternization of the tris-tertiary amine compound. The tris-tert- amine prepared in 3 above was quaternized in a procedure like those described elsewhere in this application. In a 1-liter titanium autoclave, a solution of tris-tertiary-amine in methanol (155 g. compound in 150 g. methanol) with sodium bicarbonate was purged with nitrogen and heated with methyl chloride at about 80°C until all amine had been consumed (in about 10 hours).

Filtration and evaporation yielded a brownish yellow thick paste (210 g.).

Example 5-Preparation of Amido-Bridged Multiple Functional Quaternary Ammonium Surfactant Compounds Dimeric-or higher multiple functional surfactant compounds with amide groups in the spacer groups are prepared from Duomeen (g), Triameen@, and Tetrameent) compounds from Akzo Nobel Chemicals, Inc. in the followingmanner : + dicarboxylic acid to form the bis-amido compound 4 followed by methylation, and then quaternization where R = coco-, tallow-, or oleylalkyl R = coco-, tallow-, or oleylalkyl Example 6--Preparation of Multiple Functional Quaternary Ammonium Surfactant Compounds With Ester-Groups in the Spacer from Ethoxylated Fatty Amine Compounds Various mono-and di-alkyl fatty amine compounds are available from Akzo Nobel Chemicals, Inc. and are useful as starting materials. The following route to a di-ester linked multiple functional quaternary ammonium compound can usefully be employed. H OH I Cocoalkyl-N + CH20CH2- Cocoalkyl-N Ethylene oxide Me zou 2 Cocoalkyl-N-- + HOOC COOH condensation methyla on Me

Me 0 I + Me Cocoalkyl-N,,,. I + Me! t! Me Me O Me

Example 7: Reaction of Ethoxylated Armeen 2HT with Succinic Acid.

Followed by Quaternization Ethoxylation of dialkylamine, followed by reaction with dicarboxylic acid and methylation, will yield the bis-ester-spaced bis (methyidialklyammmonium) compound.

1. Ethoxylation of Armeen 2HT In a 1-liter autoclave, Armeen 2HT (234.7 g, 0.5 mole) was dissolved in isopropyl alcohol (80 g) by heating. After nitrogen purging, ethylene oxide (22g, 0.5 mole) was introduced. The mixture was heated at 80°C <BR> <BR> <BR> <BR> for two hours. The 13C NMR indicated that the reaction was good except that some starting amine remained unreacted (HN-CH2-at 50.24 ppm).

Additional 11 g of ethylene oxide was added, and the heating at 80°C continued for two more hours. After evaporation, a white solid paste (250 g) was obtained. The product, ethoxylated Armeen 2HT, consisted of monoethoxylated amine, 71.3 mole %; polyethoxylated amine, 26.0 mole % with n = 2.7; and unreacted amine, 2.7 mole %.

2. Reaction of Ethoxylated Armeen 2HT with Succinic Acid Under an atmosphere of nitrogen, a mixture of ethoxylated Armeen 2HT (172 g, 0.3 mole), succinic acid (17.84 g, 0.15 mole) and 50% aqueous hypophosphorous acid (0.74 g) was heated with stirring at 180-5°C for 5 hours. An off-white thick paste was obtained. The product consisted of the desired diamine esters 90% and monoamines which accounted for 10% by weight.

3. Quaternization of Bis- (ethoxylated Armeen 2HT) Succinate Diester To a solution of bis- (ethoxylated Armeen 2HT) succinate (89 g, 0.14 equiv) in isopropyl alcohol (20 g) at 75-80°C, dimethyl sulfate (about 17 g, 0.135 mole) was slowly added. Free amine should be about 2% indicating substantial completion of quaternization. Evaporation yielded the neat ester diquaternary ammonium compound.

Example 8 PREPARATION OF BIS (2- ETHYLHEXYLDIMETHYLAMMONIUM)- 1.6-HEXANE Dl (CHLORIDE ! VIA BIS (SCHIFF BASE) INTERMEDIATE Summa

1. Reaction of 2-Ethylhexanal with 1 6-Hexanediamine To the melt 1,6-hexanediamine (58.1 g, 0.5 mole) at ca. 50° C, 2- ethylhexanal (128.2 g, 1 mole) was slowly added with stirring over three hours. Cooling in an ice-water bath occasionally was necessary because the reaction was exothermic. The reaction was completed as indicated by <BR> <BR> <BR> <BR> the disappearance of the aldehyde carbon in the 13C NMR spectrum. The reaction product was washed several times with deionized water.

Evaporation yielded a yellow liquid (ca 160 g) in nearly quantitative yield.

2. Reduction of Diimine with Sodium Borohydride To a solution of the diimine (g) (141.6 g, 0.38 mole) in methanol (150 g) sodium borohydride (ca 20 g) was added in small portions. During the addition, the reaction flask was cooled in an ice water bath from time to time. The reaction was completed as indicated by the disappearance of <BR> <BR> <BR> <BR> the imine carbon line at 168 ppm in the 13C NMR spectrum. The reaction mixture was washed with deionized water several times. Evaporation gave a yellowish liquid (ca 138 g).

3. Methylation of N, N'-Di (2-ethylhexyl)-1.6-hexanediamine The addition of 90% formic acid with stirring to the diamine (II) (126.3 g, 0.37 mole) yielded a light brown solution as the temperature rose to 75° C. Having been cooled to room temperature the mixture was treated with 37.1% formaldehyde solution (65.8 g, 0.814 mole) by adding the formaldehyde in small portions with stirring. The resulting mixture was evaporated on a rotary evaporator at ca 65° C for 2 hours. About 72 g of concentrated HCI was then added. The mixture was heated at 70° C for 3 hours and was then neutralized with 25% aqueous NaOH solution. The product was washed with water several times and evaporated to yield a pale yellow liquid (ca 150 g).

4. Quaternization of the di-terrtiary-amine (III) with Methyl Chloride A solution of di (tertiary amine) (147.5 g, 0.4 mole) was quaternized with methyl chloride in the presence of sodium bicarbonate (1.5 g), at 80° C for about 10 hours. The reaction was compfeted as indicated by the disappearance of the peak of the methyl carbon on nitrogen at 42.7 ppm <BR> <BR> <BR> in the 13C NMR spectrum. The reaction mixture was filtered and the filtrate was evaporated to yield the desired diquaternary ammonium satt, a pale yellow paste (189 g).

Example 9-Preparation of bis (2-ethylhexyidimethylammonium) (dimethylammonium) dihexane trichloride Summary H 0 I HwN N NiH + 2 H I I H H H I hydrogenation (V) H reductive methvlation CH-NH NH-CH (vu) (VI) CH3 quaternization with CH3C1 N CH-N N-CH- i I CH3 (VII) CH3 CH3 + cl3 CH-N + CH + N-CH 3CI- 3 CI- (VIII)

1. Reaction of di (hexamethylene) triamine with 2-Ethylhexanal Note that the"triamine"is actually a mixture of triamine and 1,6- hexanediamine. NE (neutralization equivalent) of primary amine = 96.46 ; NE (secondary amine) = 341.76 : 86% triamine, 14% diamine.

The mixture of"triamine" (101.4 g, 1.05 equivalents primary amine) and 2-ethylhexanal (134. 7g, 1.05 moles) was heated at 70° C for 4 hours. The crude product was washed with water and evaporated to yield the diimine (V) (220 g).

2. Reduction of the Diimine (V) with Sodium Borohydride <BR> <BR> <BR> <BR> <BR> <BR> <BR> To a solution of 220 g dimine (V) in methanol (220 g) was added in small portions sodium borohydride powder (20 g) until the reaction was complete as indicated by the disappearance of the imine carbon (168 ppm) in the 13C NMR spectrum. The product was washed with water and evaporated.

3. Methylation of Tris (secondary amine ! compound (Vl) To compound VI was added with stirring 90% formic acid (149 g, 2.9 moles). The temperature was maintained at 50-60° C with cooling. A 37.1 % formaldehyde solution (104 g, 1.286 moles) was added in small portions. The resulting mixture was then evaporated on a rotary evaporator to remove the excess formic acid and formaldehyde. After the addition of concentrated HCI (1.4 mole), the mixture was heated at 70° C for 3 hours and was then neutralized with 25% aqueous NaOH solution.

The product was separated, washed with water and evaporated. A pale yellow liquid (208 g) was obtained.

4. Quaternization of the Tris (tertiary amine) Compound (VII) Compound VII (140 g, 0.3 mole) dissolved in methanol (140 g), with added NaHCO3, was quaternized with methyl chloride at 80° C for 10 hours. The reaction was completed as indicated by disappearance of the methyl carbon (CH3-N) peak in the'3C NMR spectrum. Filtration and evaporation of solvent yielded a pale yellow solid (VIII) (ca. 185 g).

Example 10-Preparation of Multiple Functional Amidoamine Quaternary Ammonium Compounds: Reaction of Duomeen CD with <BR> <BR> dimethylsuccinate to form bis-Duomeen CD succinate [a bis (secondary<BR> <BR> amido-secondary amine ! compound] A mixture of Duomeen@ CD (490.8 g, 2 equivalents of primary amine) and dimethyl succinate (136.08 g, 0.93 mole) was heated at 125-130°C under nitrogen for 5 hours. Additional dimethyl succinate (6.8 g, 0.046 mole) was added and the heating was continued for another 5 hours. The bis-Duomeen succinate (XXI), an off-white solid, was obtained. The product consisted of the bis-sec-amines (95% by weight) and unreacted Duomeen (4%).

Methylation and quaternization of this bis-sec amine product can be performed in processes like those which have been described elsewhere in this application, to yield the bis (amido-amine) quaternary ammonium compound.

Example 11-Alternative Route to Multiple Functional"Internal ester" Quaternary Ammonium Compounds Step 1: Reaction of a primary fatty amine compound with formaldehyde will form the hexahydrotriazine intermediate; RNH2 + 3 HCHO e hexahydrotriazine Step 2: hexahydrotriazine is reduced to form secondary amine; Hexahydrotriazine- RNH (Me) Step 3: secondary amine is ethoyxlated to form alcohol amine compound; RNH (Me) + ethylene oxide @ RN (Me) CH2CH2OH Step 4: two equivalents of ethoxylated amine react with dicarboxylic acid to form Gemini tertiary amine; 2 RN (Me) CH2CH2OH + HOOC (CH2) 2COOH RN (Me) CH2CH200C (CH2) 2COOCH2CH2N (Me) R Step 5: Gemini tertiary amine quaternized in reaction with methylating agent (methyl chloride or methylsulfate). <BR> <BR> <BR> <BR> <BR> <BR> <BR> <P>RN (Me) CH2CH20OC (CH2) 2COOCH2CH2N (Me) R + methylating agent o Gemini"internal ester"quaternary ammonium compound Example 12-Preparation of Ester-functional tris-quaternary ammonium Compound step 1 preparation of diesteramine CH3N (CH2CH2OH) 2+ excess HOOC (CH2) 4COOL step 2 Ethoxylation of long chain amino compound (see Example 7, step 1) -OH cocoalkyl-N + CH2O CH2 o cocoalkyl-N II H CH3

step 3 Reaction of ethoxylated amine compound 11 with dicarboxylic acid I, (see Example 7, step 2) I + 2 II # followed by reductive methylation CH3 0 0 CH3 0 0 CH3 cocoalkyl-N- (CHz) z O C (CH2), C O CH2 CH2-N-CH2CH2 0 C (CH2) 4CO (CH2) 2 N cocoalkyl step 4 quaternization of III (see Example 7, step 3)