Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840298Generated: November 1, 2026

2-(Benzyloxy)-5-bromobenzaldehyde → (2-(Benzyloxy)-5-bromophenyl)methanol

https://huagongshe.com/reaction/840298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzyloxy)-5-bromobenzaldehydeHCID 733087—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product(2-(Benzyloxy)-5-bromophenyl)methanolHCID 897136—

Reaction Steps

A suspension of 2-benzyloxy-5-bromobenzaldehyde (14.5 g, 50.2 mmol) in absolute ethanol (250 ml) was treated with sodium borohydride (2.6 g, 68.8 mmol). The reaction was stirred and the temperature slowly rose to 33 ° C. After 1 hour the reaction mixture was evaporated and the residue dissolved in ethyl acetate and poured into a mixture of ice water (200 ml) and 1N HCl (25 ml). The organic layer was separated, washed with aqueous sodium hydrogen carbonate, brine, dried (Na2SO4) and evaporated to give 2-benzyloxy-5-bromobenzylalcohol as a pale yellow oil (14.85 g, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365603B1
Source datasetuspto-grants-2002_04
ORD IDord-449cd9c1a6fe4d2d974ecc19d06a1080
Source noteuspto-grants-2002_04