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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233737Generated: October 25, 2026

Sodium borohydride → (3-Fluoropyridin-2-yl)methanol

https://huagongshe.com/reaction/233737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Fluoro-2-pyridinecarboxaldehydeHCID 11344017—
SolventEthanolHCID 702—
Product(3-Fluoropyridin-2-yl)methanolHCID 1970380393%

Reaction Steps

A solution of 2-formyl-3-fluoropyridine (4.0 g, 32 mmol) and sodium borohydride (309 mg, 8 mmol) in absolute ethanol (40 mL) was stirred at 0° C. for 15 minutes and at room temperature for 1 hour. The reaction was quenched with saturated aqueous ammonium chloride (5 mL) and filtered through diatomaceous earth to remove solids. The filtrate was evaporated and the resultant white solid was dissolved in ethyl acetate and water. The aqueous layer was extracted with ethyl acetate (5×30 mL) and the combined extracts were dried over anhydrous sodium sulfate. Solvent removal provided 3.78 g (93%) of the titled product as a pale yellow oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05593993
Source datasetuspto-grants-1997_01
ORD IDord-fdf34a2ef3d04e6db937db8c77af126e
Source noteuspto-grants-1997_01