HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → N-(1-ethylthio-2,2,2-trichloroethyl)-2-acetoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-[(1,2,2,2-Tetrachloroethyl)carbamoyl]phenyl acetate | HCID 12922487 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(1-ethylthio-2,2,2-trichloroethyl)-2-acetoxybenzamide | HCID 12940123 | 90.3% |
Reaction Steps
50 ml of dichloromethane was added to 7.9 g of N-(1,2,2,2-tetrachloroethyl)-2-acetoxybenzamide. 1.3 g of ethyl mercaptan was add to the solution under stirring and then 2.0 g of triethylamine was added dropwise thereto at 10°-15° C. After effecting the reaction at room temperature for one hour, water was added thereto and the solution was allowed to stand. Then the dichloromethane layer was separated out, dried with unhydrous sodium sulfate and concentrated to obtain 7.0 g of N-(1-ethylthio-2,2,2-trichloroethyl)-2-acetoxybenzamide as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04294835 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-c718cf4be1f148179ce53d8b9f976497 |
| Source note | uspto-grants-1981_10 |