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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684536Generated: November 2, 2026

Benzoyl chloride → 1-benzoyl-6-methoxy-2H-quinoline-2-carbonitrile

https://huagongshe.com/reaction/1684536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantPotassium CyanideHCID 9032—
Reactant6-MethoxyquinolineHCID 14860—
SolventDichloromethaneHCID 6344—
Product1-benzoyl-6-methoxy-2H-quinoline-2-carbonitrileHCID 23049373.3%

Reaction Steps

A solution of 10 g (63 mmol) of 6-methoxyquinoline in 80 ml of dichloromethane is mixed with a solution of 12.4 g (188 mmol) of potassium cyanide, and 14.5 ml (125 mmol) of benzoyl chloride are then added slowly. The mixture is stirred for 18 h, the organic phase is then separated off and the aqueous phase is extracted with dichloromethane. The organic phases are washed with aqueous 5% hydrochloric acid solution and then with water, with aqueous sodium hydroxide solution and again with water, they are dried over sodium sulphate and the solvent is evaporated off under reduced pressure. The oil obtained is crystallized from 95% ethanol. 13.4 g of product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05641785
Source datasetuspto-grants-1997_06
ORD IDord-5d017520f68340f9b91e14225ca55726
Source noteuspto-grants-1997_06