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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279745Generated: October 30, 2026

Hydrochloric Acid → 2-Chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acid

https://huagongshe.com/reaction/279745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylateHCID 1235240—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acidHCID 1328274373.5%

Reaction Steps

A mixture of 116 g (0.4468 mole) of ethyl 2-chloro-4-trifluoromethyl-5-thiazolecaboxylate, 18 g (0.45 mole) of sodium hydroxide, 200 ml. of water, 400 ml. of tetrahydrofuran was stirred at room temperature for 16 hours and made acidic with 50 ml. of concentrated hydrochloric acid. The reaction mixture was extracted twice with ml. of ether. The ether-tetrahydrofuran solution was dried (MgSO4) and concentrated under reduced pressure. The residual oil was treated with benzene and the benzene solution was concentrated under reduced pressure to remove the last trace of water. The residual solid was recrystallized from hexane-benzene to give 76 g (73.4%) of 2-chloro-trifluoromethyl-5 thiazolecarboxylic acid, m.p. 131°-131.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04586948
Source datasetuspto-grants-1986_05
ORD IDord-50cf5ef5f140483482097a23a4473ba2
Source noteuspto-grants-1986_05