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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1,2,2-Tetrachloroethylsulfenyl chlorideHCID 14453—
ReactantN-(cyclohexyl)trichlorovinylsulfonamideHCID 21313256—
SolventDichloromethaneHCID 6344—
ProductN-cyclohexyl-N-(1,1,2,2-tetrachloroethylthio)trichlorovinylsulfonamideHCID 2131326472%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160845
Source datasetuspto-grants-1979_07
ORD IDord-9af11b39a9094ab785fe58e2f5ef11ef
Source noteuspto-grants-1979_07