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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 2-Trifluoromethyl-9-chloro-10,11-dihydrodibenzo[b,f]thiepin | HCID 12687120 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Trifluoromethyl-9-cyano-10,11-dihydrodibenzo[b,f]thiepin | HCID 12687122 | 14.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04228284 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-b45e66e5d02349d5bc88552696e5b023 |
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| Source note | uspto-grants-1980_10 |
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