HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602604Generated: October 27, 2026
Sodium Acetate → N-{4-chloro-2-[1-(4-fluorophenoxyimino)propyl]phenyl}trifluoromethanesulfonamide
https://huagongshe.com/reaction/602604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | O-(4-fluorophenyl)hydroxylamine hydrochloride | HCID 22120336 | — |
| Reactant | N-(4-chloro-2-propionylphenyl)trifluoromethanesulfonamide | HCID 67269822 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-{4-chloro-2-[1-(4-fluorophenoxyimino)propyl]phenyl}trifluoromethanesulfonamide | HCID 86604002 | 81% |
Reaction Steps
A solution of N-(4-chloro-2-propionylphenyl)trifluoromethanesulfonamide 22 (386 mg, 1.22 mmol), O-(4-fluorophenyl)hydroxylamine hydrochloride (200 mg, 1.22 mmol) and anhydrous NaOAc (110 mg, 1.34 mmol) in EtOH (18 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 CH2Cl2/PE, 3:2). The residue was purified by radial thin layer chromatography (eluting with CH2Cl2/PE, 1:4) to afford N-{4-chloro-2-[1-(4-fluorophenoxyimino)propyl]phenyl}trifluoromethanesulfonamide 130 (420 mg, 81%), as a pale yellow solid. M.p. 47-48° C. 1H n.m.r. (200 MHz, CDCl3) δ 11.25, br s, 1H, 7.71, d, J=8.8 Hz, 1H, 7.58, d, J=2.4 Hz, 1H, 7.40, dd, J=2.4 and 8.8 Hz, 1H, 7.18-7.02, m, 4H, 3.02, q, J=7.6 Hz, 2H, 1.31, t, J=7.6 Hz, 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-778f47c2d27a4a109d2cf4581b694c53 |
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| Source note | uspto-grants-2011_03 |
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