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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9658Generated: October 29, 2026

Sodium borohydride → {3-Methyl-5-[5-(trifluoromethyl)pyridin-2-yl]thien-2-yl}methanol

https://huagongshe.com/reaction/9658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Methyl-5-[5-(trifluoromethyl)pyridin-2-yl]thiophene-2-carbaldehydeHCID 21986306—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product{3-Methyl-5-[5-(trifluoromethyl)pyridin-2-yl]thien-2-yl}methanolHCID 21986475—

Reaction Steps

A mixture of 3-methyl-5-[5-(trifluoromethyl)pyridin-2-yl]thiophene-2-carbaldehyde (intermediate 78, 0.144 g) in tetrahydrofuran (10 ml) and water (15 ml) was treated with sodium borohydride (0.03 g). The reaction was stirred at room temperature for 30 minutes, extracted with ethyl acetate and the organic layer washed with water and dried with brine and over magnesium sulfate. The title compound was isolated after removal of the desiccant and evaporation of the solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091237B2
Source datasetuspto-grants-2006_08
ORD IDord-c4c7b667259941398d24acbf3497c507
Source noteuspto-grants-2006_08