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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210326Generated: October 31, 2026

Ammonia → 4-Thiazolemethanol, alpha-(bromomethyl)-2-(trifluoromethyl)-

https://huagongshe.com/reaction/2210326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10978660HCID 10978660—
SolventMethanolHCID 887—
Product4-Thiazolemethanol, alpha-(bromomethyl)-2-(trifluoromethyl)-HCID 22220499—

Reaction Conditions

Temperature10 °C

Reaction Steps

6 g (0.022 mol) of 2-Trifluoromethyl-4-bromoacetylthiazole are dissolved in 150 ml of methanol, and the solution is cooled to 10° C. and 0.63 g of sodium borohydride is added. After 15 minutes ice is added, and the mixture is acidified with hydrochloric acid, made alkaline with ammonia and extracted by shaking with methylene chloride. The organic phase is dried over sodium sulphate, filtered and concentrated. An oil is obtained and is reacted further as the crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457205
Source datasetuspto-grants-1995_10
ORD IDord-215bf7f683384eb69f34b746c3bfd950
Source noteuspto-grants-1995_10