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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20064Generated: October 25, 2026

3-Bromo-4-fluorobenzaldehyde → 3-Bromo-4-fluorobenzyl Alcohol

https://huagongshe.com/reaction/20064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-Bromo-4-fluorobenzyl AlcoholHCID 2773351—

Reaction Steps

3-Bromo-4-fluorobenzaldehyde (0.300 g, 1.48 mmol) was dissolved in methanol (3 mL). Sodium borohydride (0.0671 g, 1.77 mmol) was added. After 3 h, the reaction was quenched with methanol (1 mL), and the mixture was concentrated. The residue was taken up in 2:1 EtOAc-hexane (60 mL). The organic layer was extracted with dilute NaHCO3 (6 mL) then half-saturated brine (6 mL), then was dried over sodium sulfate and concentrated. The material was purified through silica gel (45 mL) using 30% to 40% EtOAc-hexane to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745484B2
Source datasetuspto-grants-2010_06
ORD IDord-16277fcba5274896b29eed960bc7b8e9
Source noteuspto-grants-2010_06