HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-bromophenyl)-1,1,1-trifluoromethanesulfonamide → HCID 69993988, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-bromophenyl)-1,1,1-trifluoromethanesulfonamide | HCID 2133889 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Product | HCID 69993988 | HCID 69993988 | 93% |
Reaction Steps
A solution of 1.52 g (5 mmol) of N-(4-bromophenyl)-C,C,C-trifluoro-methanesulphonamide (Example 13bv)) in 25 ml of ethyl orthoformate was heated to reflux for 6 hours. Subsequently, the readily volatile constituents were distilled off on a water-jet vacuum and the residue was chromatographed over a flash column with hexane/ethyl acetate 95:5. There were obtained 1.55 g (93%) of N-(4-bromophenyl)-N-ethyl-C,C,C- trifluoro-methanesulphonamide as a pale yellow oil. MS (EI): 331 and 333 (M+, 44%), 198 and 200 ([M-SO2 CF3 ]+, 80%), 118 ([M-(SO2CF3 +HBr)]+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763450 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-6d2ffc1f0a2c484785c08db57ee1fd57 |
| Source note | uspto-grants-1998_06 |