HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzenesulfonyl chloride → 2,2,2-Trifluoroethane-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(2,2,2-Trifluoroethyl)piperidine | HCID 17840004 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2,2,2-Trifluoroethane-1-sulfonamide | HCID 21265546 | 114.1% |
Reaction Steps
b)To a solution of O-protected trifluoroethyl piperidine (1.13 g, 3.6 mmol) in DCE (15 mL) was added triethylamine (0.6 mL, 4.3 mmol) then 4-chlorobenzenesulfonyl chloride (1.13 g, 5.4 mmol) and the reaction was heated at reflux overnight. The final mixture was concentrated and directly purified by flash chromatography over silica gel (eluting hexane to DCM) to afford 0.67 g (38%) of O-protected trifluoroethyl sulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208602B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-6120e816896744f9ae699066923ae09d |
| Source note | uspto-grants-2007_04 |