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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420774Generated: November 2, 2026

Benzyl Bromide → 3-Benzyloxy-4-methoxybenzaldehyde

https://huagongshe.com/reaction/1420774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantIsovanillinHCID 12127—
SolventMethanolHCID 887—
Product3-Benzyloxy-4-methoxybenzaldehydeHCID 80671—

Reaction Steps

1.2 equivalents of K2CO3 and 1.2 equivalents of benzyl bromide are added to a suspension of 0.33 mol of 3-hydroxy-4-methoxybenzaldehyde in 400 ml of methanol. After 24 hours' reflux, the reaction mixture is filtered while hot and the organic phase is then evaporated off under reduced pressure. The isolated residue is taken up in 300 ml of chloroform and then washed with water. After extraction, drying and filtration, evaporating off the organic phase under reduced pressure allows the expected product to be isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071945
Source datasetuspto-grants-2000_06
ORD IDord-f4c6219de9e84d3e88e847785f4c6db4
Source noteuspto-grants-2000_06