Method for producing fluorine-containing cyclopropane carboxylic acid compound

Patent metadata

Field	Value
Publication number	US-10793540-B2
Application number	US-201916562214-A
Country	US
Kind code	B2
Filing date	Sep 5, 2019
Priority date	Jun 29, 2015
Publication date	Oct 6, 2020
Grant date	Oct 6, 2020

Abstract

The present invention provides an industrially applicable method for production of a fluorine-containing cyclopropane carboxylic acid compound useful as an intermediate for pharmaceutical and agrichemical products. A fluorine-containing cyclopropane monoester is obtained by: forming a fluorine-containing cyclic sulfate with the use of a fluorine-containing diol compound and sulfuryl fluoride (as a cyclic sulfuric esterification step); reacting the fluorine-containing cyclic sulfate with a malonic diester, thereby forming a fluorine-containing cyclopropane diester (as a cyclopropanation step); and hydrolyzing the fluorine-containing cyclopropane diester (as a hydrolysis step). The fluorine-containing cyclopropane carboxylic acid compound, such as fluorine-containing cyclopropane monoester or its salt, can be obtained with high chemical and optical purity by mixing the fluorine-containing cyclopropane monoester with an amine and subjecting the resulting salt of the fluorine-containing cyclopropane monoester and amine to recrystallization purification.

First claim

The invention claimed is:

1. A method of producing a fluorine-containing cyclic sulfate of the general formula [2], comprising: reacting a fluorine-containing diol compound of the general formula [1] with sulfuryl fluoride in the presence of at least one basic compound selected from the group consisting of alkali metal hydrides, alkaline earth metal hydrides, alkali metal hydroxides, alkaline earth metal hydroxides, alkali metal carbonates, alkaline earth metal carbonates, alkali metal hydrogencarbonates and alkaline earth metal hydrogencarbonates

where R f represents a C 1 -C 6 linear or branched fluoroalkyl group having at least one fluorine atom; and * represents an asymmetric carbon atom

where R f represents the same group as defined in the general formula [1]; and * represents an asymmetric carbon atom.

2. The method according to claim 1 , wherein R f is a difluoromethyl group or a trifluoromethyl group.

3. The method according to claim 1 , wherein the fluorine-containing diol compound is reacted with the sulfuryl fluoride in a temperature range of −50 to +50° C.

4. The method according to claim 1 , wherein the sulfuryl fluoride is used in an amount of 0.7 to 4.0 equivalents.

5. A method of producing a fluorine-containing cyclopropane diester of the general formula [5] comprising: producing the fluorine-containing cyclic sulfate by the method according to claim 1 ; and reacting the fluorine-containing cyclic sulfate with a malonic diester of the general formula [3] in the presence of an inorganic base

where R 1 and R 2 each independently represents a C 1 -C 18 alkyl group or substituted alkyl group having a linear or branched structure or a cyclic structure (in the case of three or more carbon atoms), or a C 6 -C 18 aromatic ring group or substituted aromatic ring group

where R f represents the same group as defined in the general formula [1] of claim 1 ; R 1 and R 2 represents the same groups as defined in the general formula [3]; and * represents an asymmetric carbon atom.

6. The method according to claim 5 , wherein the inorganic base is an alkali metal, an alkali metal hydride, an alkaline earth metal hydride, an alkali metal hydroxide or an alkaline earth metal hydroxide.

7. The method according to claim 5 , wherein the fluorine-containing cyclic sulfate of the general formula [2] and the malonic diester of the general formula [3] are added into a solvent containing the inorganic base.

8. A method of producing a fluorine-containing cyclopropane monoester of the general formula [7], comprising: producing the fluorine-containing cyclopropane diester by the method according to claim 5 ; and performing hydrolysis of the fluorine-containing cyclopropane diester in the presence of an alkali metal hydroxide, an alkaline earth metal hydroxide, an alkali metal carbonate, an alkaline earth metal carbonate, an alkali metal hydrogencarbonate, an alkaline earth metal hydrogencarbonate or a quaternary ammonium hydroxide of the general formula [6]

where R 3 , R 4 , R 5 and R 6 each independently represents a C 1 -C 18 alkyl group or substituted alkyl group having a linear or branched structure or a cyclic structure (in the case of three or more carbon atoms), or a C 6 -C 18 aromatic ring group or substituted aromatic ring group; and two or more of R 3 , R 4 , R 5 and R 6 may form a part of the same aliphatic ring or aliphatic aromatic ring

where R f represents the same group as defined in the general formula [1] of claim 1 ; R 2 represents the same group as defined in the general formula [3] of claim 5 ; and * represents an asymmetric carbon atom.

9. The method according to claim 8 , wherein the hydrolysis is performed at a temperature of −30 to +40° C.

10. The method according to claim 8 , further comprising: adding an amine of the general formula [8] to the fluorine-containing cyclopropane monoester, thereby forming a salt of the fluorine-containing cyclopropane monoester and the amine as represented by the general formula [9]; and purifying the salt by recrystallization

where R 7 , R 8 and R 9 each independently represent a hydrogen atom, a C 1 -C 18 alkyl group or substituted alkyl group having a linear or branched structure or a cyclic structure (in the case of three or more carbon atoms), or a C 6 -C 18 aromatic ring group or substituted aromatic ring group

where R f represents the same group as defined in the general formula [1]; R 2 represents the same group as defined in the general formula [3] of claim 5 ; and R 7 , R 8 and R 9 represent the same groups as defined in the general formula [8].

11. The method according to claim 10 , wherein the amine of the general formula [8] is an amine of the general formula [10]:

where R 7 , R 8 and R 10 each independently represent a hydrogen atom, a C 1 -C 18 alkyl group or substituted alkyl group having a linear or branched structure or a cyclic structure (in the case of three or more carbon atoms), or a C 6 -C 18 aromatic ring group or substituted aromatic ring group; Ar 1 represents a C 6 -C 14 aromatic ring group or substituted aromatic ring group; and, when R 10 is a C 1 -C 18 alkyl group or substituted alkyl group having a linear or branched structure or a cyclic structure (in the case of three or more carbon atoms) or a C 6 -C 18 aromatic ring group or substituted aromatic ring group, * represents an asymmetric carbon atom.

12. A salt of fluorine-containing cyclopropane monoester and amine as represented by the formula [17]

where R 11 represents a C 1 -C 6 linear or branched alkyl group; R 12 , R 13 and R 14 each independently represent a hydrogen atom, or a C 1 -C 6 linear or branched alkyl group; Ar 2 represents a C 6 -C 10 aromatic ring group or substituted aromatic ring group; and, when R 14 is a C 1 -C 6 linear or branched alkyl group, * represents an asymmetric carbon atom.

Assignees

• Central Glass Co Ltd

Inventors

• Kashiwaba Takashi
• Yamazaki Takako
• Ishii Shoko
• Mimura Shunsuke
• Fushimi Masanori
• Okamoto Ryuichi
• Kobayashi Haruki
• Yasumoto Manabu

Classifications

• C07C2601/02

  with a three-membered ring · CPC title

• C07C67/52

  by change in the physical state, e.g. crystallisation · CPC title

• C07C67/343

  by increase in the number of carbon atoms · CPC title

• C07C67/313

  by introduction of doubly bound oxygen containing functional groups, e.g. carboxyl groups · CPC title

• C07C69/74

  Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring · CPC title