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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260070Generated: October 25, 2026

Benzyl Bromide → 2-(Benzyloxy)-3-methoxybenzaldehyde

https://huagongshe.com/reaction/260070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactanto-VanillinHCID 8991—
ReactantPotassium CarbonateHCID 11430—
SolventEthanolHCID 702—
Product2-(Benzyloxy)-3-methoxybenzaldehydeHCID 126808793%

Reaction Steps

A mixture of 196.0 g (1.30 mole) of o-vanillin (Aldrich), 200 g of benzyl bromide (Aldrich), 500 g of anhydrous potassium carbonate and 1,500 mL of absolute ethanol is heated, with stirring, at reflux for 6 hours. After cooling, the supernatant is decanted and the remainder is filtered. The combined filtrate and supernatant is concentrated at reduced pressure to remove solvent. The remaining oil is extracted into 1 L of ether. The ether solution is washed with 500 mL of water, 600 mL of 1% potassium hydroxide solution, and 500 mL of water and then dried (potassium carbonate) and concentrated to give 263.4 g (84% yield) of product; mp 41°-43° C. Reported mp, 43° C. (Chem. Abstr. 62:16110a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05525614
Source datasetuspto-grants-1996_06
ORD IDord-1c7d521c149d4a3c968ce07c145bcd86
Source noteuspto-grants-1996_06