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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970883Generated: October 29, 2026

Sodium Acetate → N-{2-[1-(4-chlorophenoxyimino)ethyl]-5-trifluoromethylphenyl}trifluoromethanesulfonamide

https://huagongshe.com/reaction/970883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantO-(4-chlorophenyl)hydroxylamine hydrochlorideHCID 20445467—
ReactantN-(2-acetyl-5-trifluoromethylphenyl)trifluoromethanesulfonamideHCID 86604010—
SolventEthanolHCID 702—
ProductN-{2-[1-(4-chlorophenoxyimino)ethyl]-5-trifluoromethylphenyl}trifluoromethanesulfonamideHCID 7249174690%

Reaction Steps

A solution of N-(2-acetyl-5-trifluoromethylphenyl)trifluoromethanesulfonamide 35 (250 g, 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312248B2
Source datasetuspto-grants-2007_12
ORD IDord-50da8cbac6ca435e91ca2a6e2a5a946e
Source noteuspto-grants-2007_12