HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoromethylsulfonamide → 3,4,4-trifluoro-N-[(trifluoromethyl)sulfonyl]-3-butenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoromethylsulfonamide | HCID 79001 | — |
| Reactant | 3,4,4-Trifluoro-3-butenoyl chloride | HCID 10920789 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 3,4,4-trifluoro-N-[(trifluoromethyl)sulfonyl]-3-butenamide | HCID 15335026 | 16.4% |
Reaction Steps
To an ice-cooled solution of trifluoromethanesulfonamide (2.75 g, 18.4 mmol) in 7.4 mL of 2.5 N sodium hydroxide was added 3,4,4-trifluoro-3-butenoyl chloride (2.93 g, 18.5 mmol) with stirring in 2 min. The mixture was stirred in cold for 30 min and the white precipitate formed was filtered, washed with cold water (10 mL) and dried to give 0.82 g (16%) of the desired product as a white solid. m.p. 115°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05723470 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-e1a0dc1a113c454bac338b6a5d18d9a1 |
| Source note | uspto-grants-1998_03 |