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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488911Generated: November 3, 2026

Benzyl Chloride → 4-(Benzyloxy)-3-methoxybenzoic acid

https://huagongshe.com/reaction/1488911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantVanillic AcidHCID 8468—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
Product4-(Benzyloxy)-3-methoxybenzoic acidHCID 22633557%

Reaction Steps

To a suspension of 4-hydroxy-3-methoxybenzoic acid (25 g, 0.15 mole) in ethanol (150 ml), 2N NaOH aq. (74.3 g, 0.15 mole) and benzyl chloride (56.5 g, 0.45 mole) were added, continued to stir for 1 hour under reflux. Then, 5N NaOH aq. (150 ml) was added dropwise with stirring under reflux, and continued to stir for 1 hour under reflux. After reaction, the solvent was removed, and H2O was added to the residue and acidified with conc. hydrochloric acid to make pH 1. The precipitate was filtered, washed with H2O and dried to give 22.1 g of 4-benzyloxy-3-methoxybenzoic acid as pale yellow crystals having a m.p. of 171°-172.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677112
Source datasetuspto-grants-1997_10
ORD IDord-1871826a8d8144e389c84bbf9c52f2d7
Source noteuspto-grants-1997_10