HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970869Generated: October 30, 2026
Sodium Acetate → N-{2-[(2,4-bistrifluoromethylbenzyloxyimino)methyl]-4-chlorophenyl}-trifluoromethanesulfonamide
https://huagongshe.com/reaction/970869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | O-(2,4-bistrifluoromethylbenzyl)hydroxylamine hydrochloride | HCID 86230463 | — |
| Reactant | N-(4-chloro-2-formylphenyl)trifluoromethanesulfonamide | HCID 86230476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-{2-[(2,4-bistrifluoromethylbenzyloxyimino)methyl]-4-chlorophenyl}-trifluoromethanesulfonamide | HCID 86604006 | 58% |
Reaction Steps
A solution of N-(4-chloro-2-formylphenyl)trifluoromethanesulfonamide 24 (180 mg, 0.63 mmol), O-(2,4-bistrifluoromethylbenzyl)hydroxylamine hydrochloride (342 mg, 1.16 mmol) and anhydrous NaOAc (141 mg, 1.72 mmol) in EtOH (10 mL) was stirred for 15 hours at RT. The reaction mixture was concentrated under vacuum and the residue filtered through a pad of silica (eluting with CHCl3). Purification by radial thin layer chromatography (eluting with CH2Cl2/PE, 1:9 to 3:7) afforded N-{2-[(2,4-bistrifluoromethylbenzyloxyimino)methyl]-4-chlorophenyl}-trifluoromethanesulfonamide 65 (192 mg, 58%), as a yellow solid. M.p. 65-67° C. 1H n.m.r. (200 MHz, CDCl3) δ 10.38, br s, 1H; 8.20, s, 1H; 7.97, s, 1H; 7.86, d, J=8.0 Hz, 1H; 7.75, d, J=8.0 Hz, 1H; 7.65, d, J=8.8 Hz, 1H; 7.35, dd, J=2.4 and 8.8 Hz, 1H; 7.28, d, J=2.4 Hz, 1H; 5.44, s, 2H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312248B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-6cdbd2dd75ac445ab35541835bf74a0f |
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| Source note | uspto-grants-2007_12 |
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