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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894259Generated: October 30, 2026

Quinoline → 5-Benzoylthiophene-2-carbonitrile

https://huagongshe.com/reaction/894259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
Reactant2-Bromo-5-benzoylthiopheneHCID 298604—
Product5-Benzoylthiophene-2-carbonitrileHCID 21162476—

Reaction Steps

5-Benzoyl-2-bromothiophene (8 g., 30 mmoles) and cuprous cyanide (3.2 g., 36 mmoles) were combined in 75 ml. of quinoline and refluxed for 3 hours. The reaction mixture was cooled to room temperature and solids removed by filtration with 15 ml. of quinoline and 15 ml. of water wash. The combined filtrate and washings were poured into approximately 300 g. of ice, acidified with conc. hydrochloric acid and product extracted into 300 ml. of ether. The ether extract was back-washed with 150 ml. of water, filtered from insolubles and concentrated to yield solid 5-benzoyl-2-cyanothiophene (5.7 g., m.p. 85°-89° C., m/e 213).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04282246
Source datasetuspto-grants-1981_08
ORD IDord-45d3530b5d8748929983593054f55a6d
Source noteuspto-grants-1981_08