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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261551Generated: November 4, 2026

Ammonia → 9-Cyano 10,11-dihydro-11-oxo-dibenzo[b,f]thiepin

https://huagongshe.com/reaction/261551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant1-chlorodibenzo[b,f]thiepin-10(11H)-oneHCID 827045—
ReactantHCID 178418260HCID 178418260—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
Product9-Cyano 10,11-dihydro-11-oxo-dibenzo[b,f]thiepinHCID 12687085—

Reaction Conditions

Temperature200 °C

Reaction Steps

The mixture of 2.6 g of 9-chloro-10,11-dihydro-11-oxo-dibenzo[b,f]thiepin, 2.0 g. of copper cyanide, 0.1 g of anhydrous copper sulfate and 50 ml of N-methyl pyrrolidone was heated with stirring at 200° C. overnight in a flask equipped with a tube packed with silica gel. After cooling, to the reaction mixture were added 100 ml of conc. aqueous ammonia and 200 ml of water, and the resulting mixture was extracted with benzene. The extract was washed with water, diluted hydrochloric acid and then water, which was dried over potassium sulfate and the solvent was evaporated therefrom. The residue thus obtained was chromatographed on 200 g of silica gel, and eluted with chloroform/methanol (50/1). 0.6 g of the starting material was recovered from a first eluate. Recrystallization of the residue of a second eluate from benzene gave 0.7 g of 9-cyano-10,11-dihydro-11-oxo-dibenzo[b,f]thiepin as pale yellow prismatic crystals having a melting point of 165°-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166127
Source datasetuspto-grants-1979_08
ORD IDord-139eadefe24e4298b3ca94863a7ff1d9
Source noteuspto-grants-1979_08