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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497399Generated: October 30, 2026

Sodium borohydride → (4-(Trifluoromethyl)-1,3-thiazol-2-yl)methanol

https://huagongshe.com/reaction/1497399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 4-(trifluoromethyl)thiazole-2-carboxylateHCID 23560697—
SolventMethanolHCID 887—
Product(4-(Trifluoromethyl)-1,3-thiazol-2-yl)methanolHCID 2356068883.6%

Reaction Steps

Sodium tetrahydroborate (840 mg) was added to a solution of ethyl 4-(trifluoromethyl)-1,3-thiazole-2-carboxylate (2.5 g) in methanol (15 ml) at 0° C., and the mixture was stirred at the same temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate) to give the title compound (1.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199963B2
Source datasetuspto-grants-2015_12
ORD IDord-c3705374585541c890b69f84e6009047
Source noteuspto-grants-2015_12