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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604366Generated: October 29, 2026

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

https://huagongshe.com/reaction/1604366

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 1 N 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 numberUS05994353
Source datasetuspto-grants-1999_11
ORD IDord-419696d974784e2a809d50de43d40ce7
Source noteuspto-grants-1999_11