HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602623Generated: October 31, 2026
Sodium Acetate → N-{2-[1-(4-chlorophenoxyimino)ethyl]-5-trifluoromethylphenyl}trifluoromethanesulfonamide
https://huagongshe.com/reaction/602623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | O-(4-chlorophenyl)hydroxylamine hydrochloride | HCID 20445467 | — |
| Reactant | N-(2-acetyl-5-trifluoromethylphenyl)trifluoromethanesulfonamide | HCID 86604010 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-{2-[1-(4-chlorophenoxyimino)ethyl]-5-trifluoromethylphenyl}trifluoromethanesulfonamide | HCID 72491746 | 90% |
Reaction Steps
A solution of N-(2-acetyl-5-trifluoromethylphenyl)trifluoromethanesulfonamide 35 (250 mg, 0.75 mmol), O-(4-chlorophenyl)hydroxylamine hydrochloride (148 mg, 0.82 mmol) and anhydrous NaOAc (67 mg, 0.82 mmol) in EtOH (15 mL) was stirred for 20 hours at RT. The reaction mixture was concentrated under vacuum, the residue filtered through a pad of silica (eluting with CH2Cl2) and the solvent removed under reduced pressure. The residue was purified by recrystallization from CH2Cl2/PE to afford N-{2-[1-(4-chlorophenoxyimino)ethyl]-5-trifluoromethylphenyl}trifluoromethanesulfonamide 199 (310 mg, 90%), as a pale yellow solid. M.p. 89-90° C. 1H n.m.r. (200 MHz, CDCl3) δ 11.41, br s, 1H, 8.02, s, 1H, 7.76, d, J=8.6 Hz, 1H, 7.56, m, 1H, 7.36, d, J=9.2 Hz, 2H, 7.12, d, J=9.2 Hz, 2H, 2.60, s, 3H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906538B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-34a6c7fa4a854e2d8ae07ef1c11a5f25 |
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| Source note | uspto-grants-2011_03 |
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