Description

SYNTHESIS METHOD OF METAL CYCLOPENT ADIENIDE IN

BULK

Technical Field

[1] The present invention relates to a synthesis method of metal cyclopentadienide, more precisely a synthesis method of metal cyclopentadienide in bulk by reacting dicy- clopentadiene directly with a group 1 metal using an aprotic solvent. Background Art

[2] Metal cyclopentadienide generally indicates potassium cyclopentadienide (KC H ) or sodium cyclopentadienide (NaC H ).

[3] The potassium cyclopentadienide was first synthesized by the reaction of cy- clopentadiene (Cp) and potassium (K) 100 years ago. In general, the potassium cyclopentadienide can be synthesized by reacting cyclopentadiene with potassium metal in the presence of tetrahydrofuran (THF), benzene or liquid ammonia.

[4] The synthesis of the sodium cyclopentadienide was first reported by K. Ziegler and

E. O. Fisher. And the synthesis of the sodium cyclopentadienide these days is largely induced by the reaction of cyclopentadiene and NaOH, tert-NaOtBu or NaCl.

[5] The conventional synthesis methods all use cyclopentadiene as a reactant. The cyclopentadiene is in equilibrium with dicyclopentadiene and most of the time it remains as dicyclopentadiene at room temperature.

[6] So, the cyclopentadiene is generally obtained from dicyclopentadiene by retro Diels-

Alder reaction at 17O ⁰ C. However, the synthesis method of metal cyclopentadienide by the retro Diels-Alder reaction using the dicyclopentadiene as a reactant has such problems that it is difficult to control the Diels-Alder reaction with cyclopentadiene, suggesting that dicyclopentadiene might still remain, and a process of producing cyclopentadiene has to be included, making the procedure complicated.

[7] There has been an attempt to synthesize metal cyclopentadiene not by the indirect reaction with cyclopentadiene but by direct reaction with dicyclopentadiene.

[8] Particularly, it has been tried to synthesize metal cyclopentadienide using dicyclopentadiene as a reactant in a high temperature/high pressure reactor or by the rea ction with sodium metal in the presence of iron at room temperature or at 17O ⁰ C.

[9] However, the synthesis of metal cyclopentadienide using the high temperature/high pressure reactor or via reaction using iron as a catalyst does not favor mass-production.

[10] As an alternative, a method to react dicyclopentadiene (as a reactant and reaction solvent) directly with sodium or potassium was reported in Organometallics 2003, 22, 877-878. However, this method also has a problem of over-dose of dicyclopentadiene

which is necessarily used for mass-production but has to be eliminated. Disclosure of Invention

Technical Problem

[11] It is an object of the present invention, to overcome the above problems of the conventional methods, to provide a synthesis method of metal cyclopentadienide by direct reaction of dicyclopentadiene with a group 1 metal in the presence of an aprotic solvent. Technical Solution

[12] The above object of the present invention can be achieved by the following embodiments of the present invention.

[13] The present invention is described in detail hereinafter.

[14] To achieve the above object, the present invention provides a synthesis method of metal cyclopentadienide comprising the following steps:

[15] i) adding an aprotic solvent represented by the following formula 1 (herein, R , R , R and R are substituted or unsubstituted Cl - C20 alkyl group, and n and m are equal or

4 different integers between 1 - 100.) and a group 1 metal to a reactor and raising the temperature to the boiling point of the aprotic solvent; and [16] Chemistry Figure 1

[Chem.l]

[17] ii) adding dicyclopentadiene to the reactor to induce reaction.

[18] The present invention provides a synthesis method of metal cyclopentadienide, in which the aprotic solvent represented by formula 1 and a group 1 metal are reacted in a reactor and dicyclopentadiene is added when the temperature of the reaction mixture reaches to the boiling point of the aprotic solvent and thereby the dicyclopentadiene is converted into cyclopentadiene by the aprotic solvent and further reacted with the group 1 metal added ahead of time.

[19] [Chemistry Figure 1]

[20]

[21] (Wherein, R , R , R and R are substituted or unsubstituted Cl - C20 alkyl group,

and n and m are equal or different integers between 1 - 100.)

[22] The aprotic solvent herein is preferably an ether based compound having the boiling point of 130 - 300 ⁰ C, which favors the conversion of dicyclopentadiene into cy- clopentadiene that requires at least the temperature of 13O ⁰ C. Ifa solvent with boiling point of over 300 ⁰ C is used, it is not easy to raise the reaction temperature to that boiling point.

[23] The aprotic solvent is exemplified by diethylene glycol dimethylether (diglyme), diethylene glycol dibutyl ether and diethylene glycol monomethylether. Among them, the diethylene glycol dimethylether (diglyme) represented by formula 2 is preferred.

[24] ChemistryFigure 2

[Chem.2]

[25] The synthesis process of the metal compound of cyclopentadienyl using the diglyme is as indicated in the following reaction formula 1.

[26] [Reaction Formula 1]

[28] (Wherein, M is a group 1 metal.)

[29] The group 1 metal is potassium (K) or sodium (Na).

Best Mode for Carrying Out the Invention

[30] Practical and presently preferred embodiments of the present invention are illustrative as shown in the following Examples.

[31] However, it will be appreciated that those skilled in the art, on consideration of this disclosure, may make modifications and improvements within the spirit and scope of the present invention.

[32]

[33] [Examples]

[34] Example 1 : Preparation of sodium cyclopentadienide (NaCp)

[35] To a 1OL reactor were added 4L of diglyme and 229g of sodium (lOmole) stepwise.

The temperature of the reactor was raised to the boiling point of diglyme (162 ⁰ C). After stabilizing the reaction temperature, 462g (7mole) of dicyclopentadiene was slowly added to the reaction solution. Then, white smoke was generated from the surface of the solution. Upon completion of the addition of dicyclopentadiene, reaction

was confirmed by measuring hydrogen gas generation. When hydrogen gas generation was stopped, the reaction was terminated. The resultant solution was cooled down to room temperature. A sample was taken and tested for NaCp generation by NMR. [36] ¹ H-NMR (400.13MHz, C D , ppm): δ = 5.60; ¹³ C-NMR (120.62MHz, C D , ppm): δ

6 6 6 6

= 94.9.

[37] Example 2: Preparation of potassium cvclopentadienide (KCp)

[38] An experiment was performed by the same manner as described in example 1, except that 39 Ig (lOmole) of potassium was used instead of 229g (lOmole) of sodium. The resultant solution was cooled down to room temperature. A sample was taken and tested for KCp generation by NMR. [39] ¹ H-NMR (400.13MHz, C D , ppm): δ = 5.60; ¹³ C-NMR (120.62MHz, C D , ppm): δ

6 6 6 6

= 94.9.

[40] Comparative Example 1 : Preparation of sodium cvclopentadienide (NaCp)

[41] Dicyclopentadiene was converted into cyclopentadiene by retro Diels-Alder reaction at 172 ⁰ C. To a 1OL reactor was added 6L of THF and then 229g (lOmole) of sodium was added thereto. 462g (14mole) of cyclopentadiene was slowly added to the reaction solution. Hydrogen gas generation was confirmed by using an oil bubbler. Upon completion of the addition of cyclopentadiene, hydrogen gas generation was checked by observing the oil bubbler. When hydrogen gas generation was stopped, the reaction was terminated. The generation of NaCp was confirmed by NMR. [42] ¹ H-NMR (400.13MHz, C D , ppm): δ = 5.60; ¹³ C-NMR (120.62MHz, C D , ppm): δ

6 6 6 6

= 94.9.

[43] As explained in examples, cyclopentadiene and metal cyclopentadienide were synthesized by direct addition of dicyclopentadiene at the boiling temperature of a reaction solvent. This method was confirmed to be simpler and easier than the method of comparative example in which cyclopentadiene was prepared by retro Diels-Alder reaction of dicyclopentadiene. Industrial Applicability

[44] The present invention relates to a synthesis method of metal cyclopentadienide.

According to this method, unlike the conventional method which is indirect cyclopentadiene synthesis via retro Diels-Alder reaction of dicyclopentadiene, dicyclopentadiene is directly added when the reaction temperature reaches the boiling point of a reaction solvent and thus cyclopentadiene and metal cyclopentadienide are simultaneously generated during the reaction, suggesting that the method of the invention is much more efficient.

[45]

[46] Those skilled in the art will appreciate that the conceptions and specific embodiments

disclosed in the foregoing description may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present invention. Those skilled in the art will also appreciate that such equivalent embodiments do not depart from the spirit and scope of the invention as set forth in the appended claims.