HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970884Generated: October 29, 2026
Sodium Acetate → N-{2-[1-(4-fluorophenoxyimino)ethyl]-5-trifluoromethylphenyl}trifluoromethanesulfonamide
https://huagongshe.com/reaction/970884
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | O-(4-fluorophenyl)hydroxylamine hydrochloride | HCID 22120336 | — |
| Reactant | N-(2-acetyl-5-trifluoromethylphenyl)trifluoromethanesulfonamide | HCID 86604010 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-{2-[1-(4-fluorophenoxyimino)ethyl]-5-trifluoromethylphenyl}trifluoromethanesulfonamide | HCID 72491699 | 81% |
Reaction Steps
A solution of N-(2-acetyl-5-trifluoromethylphenyl)trifluoromethanesulfonamide 35 (280 mg, 0.84 mmol), O-(4-fluorophenyl)hydroxylamine hydrochloride (150 mg, 0.92 mmol) and anhydrous NaOAc (75 mg, 0.92 mmol) in EtOH (15 mL) was stirred for 24 hours at RT. The reaction mixture was concentrated under vacuum, the residue purified by column chromatography (eluting with CH2Cl2/PE; 1:1 to 4:1) and the solvent removed under reduced pressure. Recrystallization from CH2Cl2/PE afforded N-{2-[1-(4-fluorophenoxyimino)ethyl]-5-trifluoromethylphenyl}trifluoromethanesulfonamide 200 (300 mg, 81%), as colorless crystals. M.p. 95-96° C. 1H n.m.r. (200 MHz, CDCl3) δ 11.48, br s, 1H; 8.01, s, 1H; 7.76, d, J=8.4 Hz, 1H; 7.55, m, 1H; 7.19-7.04, m, 4H; 2.60, s, 3H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07312248B2 |
|---|
| Source dataset | uspto-grants-2007_12 |
|---|
| ORD ID | ord-178ebddfdcc14fcb9f39aeb8f3a47ce6 |
|---|
| Source note | uspto-grants-2007_12 |
|---|