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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630205Generated: October 25, 2026

Sodium borohydride → (4-(Trifluoromethyl)pyridin-3-yl)methanol

https://huagongshe.com/reaction/630205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(Trifluoromethyl)pyridine-3-carbaldehydeHCID 21354724—
SolventMethanolHCID 887—
Product(4-(Trifluoromethyl)pyridin-3-yl)methanolHCID 18914105—

Reaction Steps

To a solution of sodium borohydride (324 mg, 8.6 mmol) in methanol (20 mL) was added a solution of 4-(trifluoromethyl)pyridine-3-carbaldehyde (1.0 g, 5.7 mmol) in methanol (10 mL) at 0° C. The mixture was stirred for 1.5 hours at room temperature. The solvent was evaporated, water was added, and the mixture was extracted 3 times with ethyl acetate. The combined organic phases were washed with brine and dried over sodium sulfate. After evaporation of the solvent, [4-(trifluoromethyl)pyridin-3-yl)methanol was obtained as an oil (980 mg, 97% yield) and used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315521B2
Source datasetuspto-grants-2016_04
ORD IDord-427c761b862f4dacba8eb785a1d1beb7
Source noteuspto-grants-2016_04