HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1,2,2-Tetrachloroethylsulfenyl chloride → N-isopropyl-N-(trichlorovinylthio)-chloromethanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1,2,2-Tetrachloroethylsulfenyl chloride | HCID 14453 | — |
| Reactant | Methanesulfonamide, 1-chloro-N-(1-methylethyl)- | HCID 3016718 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-isopropyl-N-(trichlorovinylthio)-chloromethanesulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04295874 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-92657f5fbe8d4675bd45b18191066f7c |
| Source note | uspto-grants-1981_10 |