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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894453Generated: November 2, 2026

Ethyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate → (2-Chloro-4-(trifluoromethyl)thiazol-5-yl)methanol

https://huagongshe.com/reaction/894453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylateHCID 1235240—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventEthanolHCID 702—
Product(2-Chloro-4-(trifluoromethyl)thiazol-5-yl)methanolHCID 1295335974%

Reaction Steps

To a mixture of 2.6 g (0.01 mol) of ethyl 2-chloro-4-(trifluoromethyl)-5-thiazolecarboxylate and 10 ml of ethanol was added. 0.62 g of sodium cyanoborohydride. The reaction mixture was stirred for 5 minutes and 0.40 g of sodium borohydride was added. The temperature of the reaction mixture raised spontaneously to boiling point. The reaction mixture was stirred for 30 minutes and quenched with water. The aqueous mixture was extracted with ether. The ether solution was dried over CaSO4 and concentrated under reduced pressure. The residue was crystallized from petroleum ether to give 1.6 g (74%) of 2-chloro-4-(trifluoromethyl)-5-thiazolemethanol, mp 39°-45° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284426
Source datasetuspto-grants-1981_08
ORD IDord-129960baedcb4b78aa4d9f3ab25777d4
Source noteuspto-grants-1981_08