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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654762Generated: October 31, 2026

Water → 3-Chlorobenzocyclobutene-1-carboxylic acid

https://huagongshe.com/reaction/654762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Chlorobicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrileHCID 13560711—
SolventEthanolHCID 702—
Product3-Chlorobenzocyclobutene-1-carboxylic acidHCID 19886375—

Reaction Steps

5.0 g of 3-chloro-1-cyanobenzocyclobutane (prepared according to the process described in Patent EP 119,107) are added to a solution of 6.0 g of potassium hydroxide in 58 ml of ethanol The mixture is stirred at room temperature overnight. 7.5 ml of water are then added and the mixture is heated to reflux for 6 hours. The ethanol is evaporated off to dryness. The residue is taken up with water and the aqueous phase is washed with ethyl ether, then acidified (pH 1) with 1N hydrochloric acid and extracted with dichloromethane. The organic phase is dried, filtered and evaporated to dryness.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05134147
Source datasetuspto-grants-1992_07
ORD IDord-68c27c083a2b4eb591ad0a191d200ae5
Source noteuspto-grants-1992_07