HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloromethanethiol → 3-(trichloromethylthio)-1,2,3-benzoxathiazin-4-(3H)-one 2-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloromethanethiol | HCID 6390 | — |
| Reactant | 2-Oxobenzo[e]oxathiazin-4-one | HCID 12220829 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(trichloromethylthio)-1,2,3-benzoxathiazin-4-(3H)-one 2-oxide | HCID 21440871 | 40.1% |
Reaction Steps
A 300-ml flask equipped with a stirrer and thermomether was charged with 5.0 g (0.03 mol) of 1,2,3-benzoxthiazin-4-(3H)-one 2-oxide, 5.3 g (0.03 mol) of perchloromethyl mercaptan, 3.1 g (0.03 mol) of thiethylamine and 150 ml of methylene chloride. The resulting mixture was stirred at ambient temperature for 1 hour. At the end of this time, the reaction mixture was filtered and washed 3 times with equal amounts of water. After drying, the solvent was removed by evaporation. The crude product was passed through a 250-g silica-gel column using hexane, 10% ether/hexane, and 20% ether/hexane, respectively. Evaporation gave 4 g of 3-(trichloromethylthio)-1,2,3-benzoxathiazin-4-(3H)-one 2-oxide having a melting point of 65°-67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04018920 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-2aed3fc981ea458aa0648f96ade10e6d |
| Source note | uspto-grants-1977_04 |