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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689413Generated: October 30, 2026

Water → 3-(Carboxymethyl)-2-chlorobenzoic acid

https://huagongshe.com/reaction/1689413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Chloro-3-(cyanomethyl)benzoic acidHCID 57989381—
SolventEthanolHCID 702—
Product3-(Carboxymethyl)-2-chlorobenzoic acidHCID 57988967—

Reaction Steps

Potassium hydroxide (2.976 g) in water (30 mL) was added to a suspension of 2-chloro-3-(cyanomethyl)benzoic acid (example 80, step a) (4.12 g) in ethanol (30 mL) and the resulting solution was heated at reflux for 2 hours, then allowed to cool overnight. 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 three times with ethyl acetate. The combined extracts were dried over anhydrous magnesium sulphate and concentrated in vacuo to afford the crude subtitled compound as a yellow solid. Yield 4.11 g. Used directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-266f45c09231452b80e4de0c57b85fd9
Source noteuspto-grants-2012_04