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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869363Generated: November 2, 2026

Potassium Cyanide → (3-Chloro-2-methoxyphenyl)acetonitrile

https://huagongshe.com/reaction/1869363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantN-bromobutanimideHCID 67184—
Reactant1-Chloro-2-methoxy-3-methylbenzeneHCID 13434577—
CatalystBenzoyl PeroxideHCID 7187—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
Product(3-Chloro-2-methoxyphenyl)acetonitrileHCID 1798927781.1%

Reaction Steps

39.4 g (221.3 mmol) of NBS and 100 mg of benzoyl peroxide are added to 31.6 g (201.7 mmol) of 3-chloro-2-methoxytoluene in 500 ml of CCl4. It is refluxed over 16 hours, allowed to cool and filtered. Solvent is removed from the filtrate, and the filtrate is dissolved in 214 ml of N,N-dimethylformamide and 142 ml of water. 20.9 g (322.1 mmol) of potassium cyanide is added at 0° C. and stirred over 16 hours. The reaction mixture is diluted with water and extracted several times with tert-butyl-methyl ether. The organic phase is washed several times with saturated sodium chloride solution and dried on sodium sulfate. The solvent is removed in a vacuum and after chromatographic purification on silica gel (hexane/ethyl acetate 20%), 29.7 g of product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638515B2
Source datasetuspto-grants-2009_12
ORD IDord-16bcc6ebf8a9424d8fde0ef01c3a40c1
Source noteuspto-grants-2009_12