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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844594Generated: October 26, 2026

Water → 3-(Benzyloxy)-4-chlorobenzoic acid

https://huagongshe.com/reaction/1844594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-3-hydroxybenzoic acidHCID 141872—
SolventDimethylformamideHCID 6228—
Product3-(Benzyloxy)-4-chlorobenzoic acidHCID 67216991—

Reaction Steps

2.67 ml benzylbromide are added dropwise to 1.73 g 3-hydroxy-4-chloro-benzoic acid and 3.04 g potassium carbonate in 10 ml N,N-dimethylformamide, and the reaction mixture is stirred overnight at ambient temperature. Then the reaction mixture is mixed with water and extracted with ethyl acetate. The combined organic phases are dried on magnesium sulphate and evaporated down. The flask residue is taken up in 5 ml of methanol, combined with 3 ml of 10 M aqueous potassium hydroxide solution and stirred for 4 h at 50° C. gerührt. The reddish solution is diluted with water and acidified with 3 N aqueous hydrochloric acid. The precipitate formed is suction filtered, washed with water and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946438B2
Source datasetuspto-grants-2015_02
ORD IDord-49c4c03e33e34e78835e430583f9ea91
Source noteuspto-grants-2015_02