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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370116Generated: October 30, 2026

3-Bromo-4-methoxybenzaldehyde → (3-Bromo-4-methoxyphenyl)methanol

https://huagongshe.com/reaction/1370116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-methoxybenzaldehydeHCID 98662—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product(3-Bromo-4-methoxyphenyl)methanolHCID 1355134699.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-bromo-4-methoxybenzaldehyde (4.98 g) in ethanol (50 mL) and tetrahydrofuran (10 mL) was added sodium borohydride (1.31 g) under ice-water cooling. The mixture was stirred at 0° C. for 2 hours. After evaporation of the solvent, the residue was partitioned between ethyl acetate and water. The separated organic layer was washed successively with water and brine, and dried over magnesium sulfate. The organic layer was evaporated in vacuo to give 3-bromo-4-methoxybenzyl alcohol as a colorless oil (4.98 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06582351B1
Source datasetuspto-grants-2003_06
ORD IDord-7f78ab457c67489ab445aa5a1d7bd82d
Source noteuspto-grants-2003_06