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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203118Generated: November 2, 2026

Sodium borohydride → [2-(Difluoromethyl)-1,3-thiazol-4-yl]methanol

https://huagongshe.com/reaction/2203118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 2-(difluoromethyl)thiazole-4-carboxylateHCID 89690438—
SolventMethanolHCID 887—
Product[2-(Difluoromethyl)-1,3-thiazol-4-yl]methanolHCID 8969000555.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl 2-(difluoromethyl)thiazole-4-carboxylate (100 mg) in MeOH (1 ml) was added NaBH4 (36.5 mg) at 0° C., and the mixture was stirred at 0° C. for 3 h. The mixture was quenched with saturated NH4Cl solution, and extracted with EtOAc. The organic layer was separated, washed with water and brine successively, dried over MgSO4 and concentrated in vacuo. The residue was purified by NH silica gel column chromatography (hexane/EtOAc) to give the title compound (44.0 mg) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365540B2
Source datasetuspto-grants-2016_06
ORD IDord-a88d85b481a546f38eaf70549a923a48
Source noteuspto-grants-2016_06