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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866930Generated: October 30, 2026

N-methyl-2-pyrrolidone → 2-Trifluoromethyl-9-cyano-10,11-dihydrodibenzo[b,f]thiepin

https://huagongshe.com/reaction/866930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant2-Trifluoromethyl-9-chloro-10,11-dihydrodibenzo[b,f]thiepinHCID 12687120—
ReactantAzane;hydrateHCID 12896473—
ReactantHCID 178418260HCID 178418260—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
Product2-Trifluoromethyl-9-cyano-10,11-dihydrodibenzo[b,f]thiepinHCID 1268712214.7%

Reaction Steps

The mixture of 450mg of 2-trifluoromethyl-9-chloro-10,11-dihydrodibenzo[b,f]thiepin, 0.4g of copper cyanide, 0.05g of anhydrous copper sulfate and 10ml of N-methylpyrrolidone was stirred at 180° to 210° C for 18.5 hrs. while preventing the moisture. A ter cooling, to the mixture was added 2.5ml of conc. ammonia water and 35ml of water and the resulting mixture was filtered with the use of celite. The thus obtained solution was extracted with benzene and the extract was washed with water and dried over anhydrous sodium sulfate. The solvent was evaporated to obtain 0.3g of a brown oily substance, which was chromatographed on a silica gel, eluted with n-hexane, and there was obtained 64mg of the desired product. This was recrystallized from n-hexane to afford 2-trifluoromethyl-9-cyano-10,11-dihydrodibenzo-[b,f]thiepin having a melting point of 113° to 114.5° C as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101667
Source datasetuspto-grants-1978_07
ORD IDord-733c04bf11f445a1a1c130fbd8cb70f2
Source noteuspto-grants-1978_07