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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471182Generated: October 26, 2026

Potassium Cyanide → 2-Chloro-3-(cyanomethyl)benzoic acid

https://huagongshe.com/reaction/471182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant3-(Bromomethyl)-2-chlorobenzoic acidHCID 20221490—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Chloro-3-(cyanomethyl)benzoic acidHCID 57989381—

Reaction Steps

A solution of 3-(bromomethyl)-2-chlorobenzoic acid (6.39 g) in DMF (75 mL) was treated with a solution of potassium cyanide (3.34 g) in water (25 mL) and the resulting solution was stirred at room temperature overnight. The mixture was diluted with water and extracted twice with ethyl acetate. The organic phases were discarded, whilst the aqueous phase was carefully acidified with concentrated hydrochloric acid (25 mL), venting any liberated HCN through a bleach solution via a stream of nitrogen. After being stirred for 2 hours, the aqueous phase was extracted twice more with ethyl acetate. The combined organic phases were washed three times with water, once with brine, then dried over anhydrous magnesium sulphate and concentrated in vacuo to afford the crude subtitled compound as a pale brown solid. Yield 4.12 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629271B2
Source datasetuspto-grants-2014_01
ORD IDord-d19e8d937a874c1c83985ff7a18d0fb7
Source noteuspto-grants-2014_01