HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → N-[2-(1-allyloxyiminoethyl)-5-trifluoromethylphenyl]trifluoromethanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | O-Allylhydroxylamine hydrochloride | HCID 3084724 | — |
| Reactant | N-(2-acetyl-5-trifluoromethylphenyl)trifluoromethanesulfonamide | HCID 86604010 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[2-(1-allyloxyiminoethyl)-5-trifluoromethylphenyl]trifluoromethanesulfonamide | HCID 73038538 | 80% |
Reaction Steps
A solution of N-(2-acetyl-5-trifluoromethylphenyl)trifluoromethanesulfonamide 35 (168 mg, 0.50 mmol), O-allylhydroxylamine hydrochloride (60mg, 0.53 mmol) and anhydrous NaOAc (43 mg, 0.53 mmol) in EtOH (3 mL) was stirred for 15 hours at RT. The reaction mixture was concentrated under vacuum, and the residue purified by radial thin layer chromatography (eluting with CH2Cl2/PE, 1:99) to afford N-[2-(1-allyloxyiminoethyl)-5-trifluoromethylphenyl]trifluoromethanesulfonamide 241 (155 mg, 80%), as a colorless oil. 1H n.m.r. (400 MHz, CDCl3) δ 11.82, br s, 1H; 7.98, s, 1H; 7.65, d, J=8.2Hz, 1H; 7.49, d, J=8.2Hz, 1H; 6.02, m, 1H; 5.44, d, 3J=17.2 Hz, 1H; 5.37, d, 3J=10.4 Hz, 1H; 4.72, d, J=6.0 Hz, 2H; 2.38, s, 3H. HRMS (M+) 390.0465.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07312248B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-3229c286f99a4063925efc1d2de3b184 |
| Source note | uspto-grants-2007_12 |