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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610344Generated: October 30, 2026

Water → (2-(Trifluoromethyl)-1,3-thiazol-5-yl)methanol

https://huagongshe.com/reaction/1610344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(trifluoromethyl)-1,3-thiazole-5-carboxylateHCID 15171126—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(2-(Trifluoromethyl)-1,3-thiazol-5-yl)methanolHCID 15171127—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of lithium aluminum hydride (2.17 g, 57.1 mmol) in tetrahydrofuran (80 ml) was dropwise added a solution of ethyl 2-(trifluoromethyl)-1,3-thiazole-5-carboxylate (8.579 g, 38.10 mmol) in tetrahydrofuran (40 ml) under ice-cooling and the mixture was stirred at 0° C. 1 hr. The reaction solution was ice-cooled and water (2 ml), 15% aqueous sodium hydroxide solution (2 ml) and water (5 ml) were dropwise added successively to decompose excess lithium aluminum hydride. The mixture was stirred at room temperature as it was for 2 hrs. The resulting precipitate was removed by filtration and the precipitate was washed with ethyl acetate. The solvent of the collected filtrate was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=6/1−1/1) to give the objective substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-bc65fcba86a64cfdbd907f1a3373e014
Source noteuspto-grants-2006_01