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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35283Generated: October 26, 2026

Benzyl Bromide → 5-(Benzyloxy)-2-methoxybenzaldehyde

https://huagongshe.com/reaction/35283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium HydroxideHCID 14798—
Reactant5-Hydroxy-2-MethoxybenzaldehydeHCID 358341—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-(Benzyloxy)-2-methoxybenzaldehydeHCID 1096669491%

Reaction Steps

To a stirred suspension of 5-hydroxy-2-methoxybenzaldehyde (306.6 g, prepared by the method of Ulrich et al, J.Org.Chem., 1974, 39, 2437), benzyl bromide (355.8 g) and Adogen 464 (48.5 g) in dichloromethane (600 ml) was added a solution of sodium hydroxide (123.5 g) in water (500 ml). The mixture became warm and the suspension dissolved; additional dichloromethane (300 ml) was added to prevent crystallisation of the benzylated product. After 2 hours, the organic layer was removed, washed twice with water, once with saturated sodium chloride solution, then dried with anhydrous magnesium sulphate. The solution was concentrated, then treated with petroleum spirit to give 5-benzyloxy-2-methoxybenzaldehyde (445.7 g, 91%), m.p. 99°-100°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766121
Source datasetuspto-grants-1988_08
ORD IDord-09acaa2b0fe944e185cdd2596e974e13
Source noteuspto-grants-1988_08