Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903648Generated: October 31, 2026

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

https://huagongshe.com/reaction/903648

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 450 mg of 2-trifluoromethyl-9-chloro-10,11-dihydrodibenzo[b,f]thiepin, 0.4 g of copper cyanide, 0.05 g of anhydrous copper sulfate and 10 ml of N-methylpyrrolidone was stirred at 180° to 210° C. for 18.5 hrs. while preventing the moisture. After cooling, to the mixture was added 2.5 ml of conc. ammonia water and 35 ml 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 0.3 g of a brown oily substance, which was chromatographed on a silica gel, eluted with n-hexane, and there was obtained 64 mg 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 numberUS04228284
Source datasetuspto-grants-1980_10
ORD IDord-b45e66e5d02349d5bc88552696e5b023
Source noteuspto-grants-1980_10