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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848398Generated: October 30, 2026

1,1,2,2-Tetrachloroethylsulfenyl chloride → N-isopropyl-N-(trichlorovinylthio)-chloromethanesulfonamide

https://huagongshe.com/reaction/848398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,2,2-Tetrachloroethylsulfenyl chlorideHCID 14453—
ReactantMethanesulfonamide, 1-chloro-N-(1-methylethyl)-HCID 3016718—
SolventTriethylamineHCID 8471—
ProductN-isopropyl-N-(trichlorovinylthio)-chloromethanesulfonamideHCID 12943924—

Reaction Steps

A 32.3 g (0.32 mol) sample of triethylamine was added dropwise to a cooled (0° C.) solution of 50 g (0.29 mol) N-isopropyl chloromethanesulfonamide and 70 g (0.29 mol) 1,1,2,2-tetrachloroethylsulfenyl chloride. After the addition was completed, the reaction was stirred at ambient temperature for 30 minutes and then under reflux for 3 hours. The reaction mixture was then cooled, washed with water, dried over magnesium sulfate and evaporated under reduced pressure to give the N-isopropyl-N-(trichlorovinylthio)-chloromethanesulfonamide product, which after crystallization from pet. ether melted at 71°-73° C. The product is reported as Compound 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04295874
Source datasetuspto-grants-1981_10
ORD IDord-92657f5fbe8d4675bd45b18191066f7c
Source noteuspto-grants-1981_10