HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971648Generated: October 26, 2026
Triethylamine → N-cyclohexyl-N-(1,1,2,2-tetrachloroethylthio)trichlorovinylsulfonamide
https://huagongshe.com/reaction/971648
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1,2,2-Tetrachloroethylsulfenyl chloride | HCID 14453 | — |
| Reactant | N-(cyclohexyl)trichlorovinylsulfonamide | HCID 21313256 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-cyclohexyl-N-(1,1,2,2-tetrachloroethylthio)trichlorovinylsulfonamide | HCID 21313264 | 72% |
Reaction Steps
A 4.0 g (0.04 mol) sample of triethylamine was added dropwise to a cooled (-10° to 0° C.) solution of 9.5 g (0.0324 mol) N-(cyclohexyl)trichlorovinylsulfonamide, m.p. 152°-153° C., and 7.6 g (0.0324 mol) 1,1,2,2-tetrachloroethylsulfenyl chloride in 200 ml dichloromethane. The reaction mixture was then stirred at about 25° C. for 3 hours, washed with water, dried over magnesium sulfate and evaporated to give an oil. The oil was chromatographed on silica gel. The N-cyclohexyl-N-(1,1,2,2-tetrachloroethylthio)trichlorovinylsulfonamide product, 11 g (72% yield), was eluted from the silica gel with 30% ether/20% hexane. The infrared spectrum of the product showed strong absorption bands at 1385 cm-1 and 1160 cm-1. The elemental analysis for the product is tabulated in Table I under Compound No. 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04160845 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-9af11b39a9094ab785fe58e2f5ef11ef |
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| Source note | uspto-grants-1979_07 |
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