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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657166Generated: October 28, 2026

3,5-Dibromobenzaldehyde → (3,5-Dibromophenyl)methanol

https://huagongshe.com/reaction/1657166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DibromobenzaldehydeHCID 622077—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product(3,5-Dibromophenyl)methanolHCID 7009423—

Reaction Steps

1.14G(30 mM) of sodium borohydride was added slowly to a suspension of 3,5-dibromobenzaldehyde (7.92G; 30 mM), from step (a), in 50 mL of methanol at 0° under nitrogen. After stirring 30 mins., the reaction mixture was diluted with 150 mL of ethyl acetate and washed with 5×50 mL of saturated sodium chloride solution, dried over anhydrous magnesium sulfate. Solvent removal afforded a crude product, which was dissolved in minimum amount of CH2Cl2 and applied on silica gel. Elution with 1:2 mixture of EtOAc:hexane gave 7.2G of the desired alcohol as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256777
Source datasetuspto-grants-1993_10
ORD IDord-1bccf3eb2bd541c6aa1451531fc02844
Source noteuspto-grants-1993_10