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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203012Generated: October 30, 2026

Methanol → 5-(Trifluoromethyl)-3-thiophenemethanol

https://huagongshe.com/reaction/2203012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 5-(trifluoromethyl)thiophene-3-carboxylateHCID 89690311—
SolventTetrahydrofuranHCID 8028—
Product5-(Trifluoromethyl)-3-thiophenemethanolHCID 1995739399.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of methyl 5-(trifluoromethyl)thiophene-3-carboxylate (523 mg) in THF (1 ml)-MeOH (1 ml) was added NaBH4 (2.2 g) at room temperature, and the reaction mixture was stirred at 60° C. for 3 h. The reaction mixture was quenched with water, and extracted with EtOAc. The extract was washed with brine, dried over MgSO4, concentrated and purified by silica gel column chromatography (hexane/EtOAc) to give the title compound (449 mg) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365540B2
Source datasetuspto-grants-2016_06
ORD IDord-1e2c80422bdb4179887d3c9cdb8d9899
Source noteuspto-grants-2016_06