Process for preparing racemic alkyl-5-halopent-4-enecarboxylic acids or carboxylic esters
View Patent ↗A process for preparing racemic alkyl-5-halopent-4-enecarboxylic acids and esters thereof of the formula (I), in which R is a C 1 -C 6 -alkyl radical, R 1 is H or C 1-4 -alkyl and X is chlorine, bromine or iodine, which comprises a) reacting a dialkyl alkylmalonate of the formula (II),in which R is as defined above and R 2 is a C 1 -C 4 -alkyl radical, in the presence of a metal alkoxide of the formula MOR 3 , in which M may be Na, K or Li, and R 3 is a C 1 -C 4 -alkyl radical, and in an organic solvent, with 1,3-dihalopropene to give the corresponding allylated malonate, then b) after full conversion, adding an inorganic salt and a C 1 -C 6 alcohol to the reaction mixture, heating the reaction mixture to reflux temperature, then c) isolating the desired racemic ester of the formula (I) from the reaction mixture by extraction or direct distillation and d) if the racemic acid is the desired end product, hydrolyzing the ester function.
1. A process for preparing racemic alkyl-5-halopent-4-enecarboxylic acids and esters thereof of the formula (I)
in which R is a C 1 -C 6 alkyl radical, R 1 is H or C 1 -C 4 -alkyl and X is chlorine, bromine or iodine, which comprises:
a) reacting a dialkyl alkylmalonate of the formula (II)
in which R is as defined above and R 2 is a C1-C4-alkyl radical, in the presence of a metal alkoxide of the formula MOR 3, in which M may be Na, K or Li, and R 3 is a C 1 -C 4 -alkyl radical, and in an organic solvent, with 1,3-dihalopropene to give the corresponding allylated malonate, then
b) after full conversion, adding an inorganic salt and a C 1 -C 6 alcohol to the reaction mixture, heating the reaction mixture to reflux temperature, then
c) isolating the desired racemic ester of the formula (I) from the reaction mixture by extraction or direct distillation and
d) if the racemic acid is the desired end product, hydrolyzing the ester function.
2. The process as claimed in claim 1 , wherein 1,3-dihalopropene is used in step a) in an amount of from 0.8 to 1.5 molar equivalents and the metal alkoxide in an amount of from 0.6 to 1.3 molar equivalents, based in each case on the malonate of the formula (II).
3. The process as claimed in claim 1 , wherein the 1,3-dihalopropene used is 1,3-dichloropropene.
4. The process as claimed in claim 1 , wherein the inorganic salt used in step b) is a salt from the group of LiCl, CaCl 2 , MgCl 2 , NaCl 1 NaBr, LiCN or NaCN, and the alcohol used is a C 1 -C 4 alcohol.
5. The process as claimed in claim 1 , wherein the inorganic salt is used in step b) in an amount of from 0.1 to 1.5 molar equivalents and the alcohol in an amount of from 1.0 to 3.0 molar equivalents, based in each case on the allylated malonate.
6. The process as claimed in claim 1 , wherein the dialkyl alkylmalonate of the formula (II) is first prepared by reacting a corresponding dialkyl malonate of the formula (III)
in which R 2 is as defined above with an alkyl halide of the formula R-X, where X is bromine, chlorine, iodine and R is as defined above in a suitable solvent in the presence of a metal alkoxide of the formula MOR3 in which M may be Na, K or Li and R 3 is a C 1 -C 4 -alkyl radical.
7. The process as claimed in claim 6 , wherein the halide is used in an amount of from 0.8 to 1.5 molar equivalents and the metal alkoxide in an amount of from 0.8 to 1.5 molar equivalents, based in each case on the malonate of the formula (III).
8. The process as claimed in claim 1 , wherein the malonate of the formula (II) is purified by distillation by means of a column under reduced pressure before the reaction with 1,3-dihalopropene.
9. The process as claimed in claim 1 , wherein the racemic acids and esters thereof according to formula (I) are obtained in a yield of up to 98% of theory.
10. The process as claimed in claim 1 , wherein the racemic acids and esters thereof according to formula (I) are obtained in a yield of 79% up to 98% of theory.