HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2-(2-Fluoroethylthio)-phenylsulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-(2-fluoroethylthio)-N-tert.-butylphenylsulfonamide | HCID 19910936 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(2-Fluoroethylthio)-phenylsulfonamide | HCID 19809754 | — |
Reaction Steps
25 ml of trifluoroacetic acid are added at a temperature of 0° C. to a solution of 3.88 g of 2-(2-fluoroethylthio)-N-tert.-butylphenylsulfonamide, obtained in accordance with Example P1, in 25 ml of trichloromethane. After stirring for 18 hours at a temperature of +25° C., the resulting brown reaction mixture is lyophilised. After chromatographic purification of the oily residue with 1) ethyl acetate/petroleum ether (1:1) over silica gel and 2) dichloromethane/acetone (9:1) over silica gel, the resulting fractions are concentrated by evaporation to give 1.5 g (60.5% of the theoretical yield) of crystalline 2-(2-fluoroethylthio)-phenylsulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05087749 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-8c7a26a5f0f042409d8bf6feb52d9d17 |
| Source note | uspto-grants-1992_02 |