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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295406Generated: October 31, 2026

Hydrochloric Acid → 2-{[2-Chloro-4-(trifluoromethyl)phenyl]amino}-3-methylbutanoic acid

https://huagongshe.com/reaction/2295406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfolaneHCID 31347—
ReactantBenzene, 2-chloro-1-fluoro-4-(trifluoromethyl)-HCID 157153—
ReactantHCID 23706288HCID 23706288—
SolventWaterHCID 962—
Product2-{[2-Chloro-4-(trifluoromethyl)phenyl]amino}-3-methylbutanoic acidHCID 394764396%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 10 parts of 3-chloro-4-fluorobenzotrifluoride, 10 parts of potassium valinate and 50 parts of sulfolane was heated and maintained at about 125° C. for about 17 hours, with mixing. The mixture was then cooled to room temperature, diluted with water and acidified with hydrochloric acid to a pH of 1.0. The aqueous layer was extracted with diethyl ether. The ether layers were washed with water, then dried and concentrated by evaporation to yield 9.6 parts of 2-(2-chloro-4-trifluoromethylphenylamino)-3-methylbutanoic acid (96% purity); a yield of about 65% based on the 3-chloro-4-fluorobenzotrifluoride starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04424396
Source datasetuspto-grants-1984_01
ORD IDord-471c87b11b8a4c008f06765db3f8d0a9
Source noteuspto-grants-1984_01