HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(4,5,7-trifluorobenzothiazol-2-ylthio)-N-phenylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Chloroacetanilide | HCID 11485 | — |
| Reactant | HCID 178505914 | HCID 178505914 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4,5,7-trifluorobenzothiazol-2-ylthio)-N-phenylacetamide | HCID 21463540 | 54.7% |
Reaction Steps
To DMSO (15 ml) was added α-chloroacetoanilide (850 mg, 5 mmol), 4,5,7-trifluoro-2-mercaptobenzothiazole (1.1 g, 5 mmol), potassium carbonate (690 mg, 5 mmol) and potassium iodide (50 mg) and the mixture was stirred at room temperature for 4 hours. The resultant reaction mixture was diluted with water, acidified with 7% hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, dried and then evaporated to yield a crude product, which was purified on a silica gel column to give 2-(4,5,7-trifluorobenzothiazol-2-ylthio)-N-phenylacetamide (0.97 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05700819 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-ee2697d21caa4e5999c13043483e5995 |
| Source note | uspto-grants-1997_12 |