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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689390Generated: November 2, 2026

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

https://huagongshe.com/reaction/1689390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Chloro-3-(cyanomethyl)benzoic acidHCID 66964149—
SolventEthanolHCID 702—
Product3-(Carboxymethyl)-4-chlorobenzoic acidHCID 57989320—

Reaction Steps

Potassium hydroxide (1.549 g) in water (15 mL) was added to a suspension of 4-chloro-3-(cyanomethyl)benzoic acid (2.07 g) in ethanol (15 mL) and the resulting solution was heated at reflux for 4 hours, then allowed to cool. The mixture was concentrated in vacuo to remove the ethanol and then diluted with water and washed twice with ethyl acetate. The organic phases were discarded, whilst the aqueous phase was acidified to pH 1 with concentrated hydrochloric acid and extracted twice with ethyl acetate. The combined extracts were washed with brine, dried over anhydrous magnesium sulphate and concentrated in vacuo to afford the subtitled compound as a pale brown solid. Yield 2.06 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-93970828c2fd44fe9dd93a00d6538a9a
Source noteuspto-grants-2012_04