HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 15766992, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Chlorobenzenesulfonamide | HCID 81410 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15766992 | HCID 15766992 | — |
Reaction Steps
62 g (1.0 mol) of ethanethiol were added to a mixture of 65.9 g (1.0 mol) of 85% strength potassium hydroxide powder and 500 ml of dimethylformamide at 25° C. while stirring, and stirring was continued for 15 minutes. Thereafter, a solution of 95.8 g (0.5 mol) of 2-chlorobenzenesulfonamide was added at 90° C. while stirring in the course of 30 minutes, and stirring was continued for 8 hours at 110° C. The mixture was cooled and was evaporated down under reduced pressure, after which the residue was partitioned between methylene chloride and water, and the organic phase was washed with dilute sodium chloride solution. Evaporating down under reduced pressure gave 88.4 g (81.5% of theory) of the title compound as a semicrystalline mass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05591694 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-3e35b02698ff411d844f6d5169bdedff |
| Source note | uspto-grants-1997_01 |