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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantO-(4-fluorophenyl)hydroxylamine hydrochlorideHCID 22120336—
ReactantN-(2-acetyl-5-trifluoromethylphenyl)trifluoromethanesulfonamideHCID 86604010—
SolventEthanolHCID 702—
ProductN-{2-[1-(4-fluorophenoxyimino)ethyl]-5-trifluoromethylphenyl}trifluoromethanesulfonamideHCID 7249169981%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312248B2
Source datasetuspto-grants-2007_12
ORD IDord-178ebddfdcc14fcb9f39aeb8f3a47ce6
Source noteuspto-grants-2007_12