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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377550Generated: October 31, 2026

Ethyl trifluoroacetate → 2,2,2-Trifluoro-1-(4-methyl-1,3-thiazol-2-yl)ethan-1-one

https://huagongshe.com/reaction/1377550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
Reactant4-MethylthiazoleHCID 12748—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2,2,2-Trifluoro-1-(4-methyl-1,3-thiazol-2-yl)ethan-1-oneHCID 22106690—

Reaction Steps

n-Butyllithium (2.5M solution in hexanes, 40.4 ml) was added dropwise to a stirred solution of 4-methylthiazole (10 g) in anhydrous tetrahydrofuran at -70° C. under an atmosphere of dry nitrogen. After 30 minutes, ethyl trifluoroacetate (12 ml) was added dropwise. After a further 2 hours the mixture was allowed to warm to room temperature and was then left stirring overnight. Saturated aqueous ammonium chloride solution was added and the organic phase was separated, dried and evaporated to dryness. The residue was purified by flash chromatography to give the hydrate corresponding to the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665747
Source datasetuspto-grants-1997_09
ORD IDord-dc67baae4ea3436781168a0ee74b9e38
Source noteuspto-grants-1997_09