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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970867Generated: October 30, 2026

Acetic Acid → N-{4-chloro-2-[1-(thiophen-2-ylmethoxyimino)propyl]phenyl}trifluoromethanesulfonamide

https://huagongshe.com/reaction/970867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant2-(2-Thienylmethoxy)-1H-isoindole-1,3(2H)-dioneHCID 10706403—
ReactantN-(4-chloro-2-propionylphenyl)trifluoromethanesulfonamideHCID 67269822—
SolventEthanolHCID 702—
ProductN-{4-chloro-2-[1-(thiophen-2-ylmethoxyimino)propyl]phenyl}trifluoromethanesulfonamideHCID 8660400585.3%

Reaction Steps

N,N-Dimethylethylenediamine (254 μL, 2.20 mmol) was added to a solution of N-(thiophen-2-ylmethoxy)phthalimide (365 mg, 1.50 mmol) in EtOH (5 mL), and the reaction allowed to stir at RT for 15 h. Glacial acetic acid (1 mL) was then added to adjust the mixture to ca. pH 4 followed by a solution of N-(4-chloro-2-propionylphenyl)trifluoromethanesulfonamide 22 (316 mg, 1.0 mmol) in EtOH (2 mL), and the mixture stirred for 15 h at RT. The reaction mixture was concentrated under vacuum, and the residue purified by column chromatography (eluting with CH2Cl2/PE, 1:1) to afford N-{4-chloro-2-[1-(thiophen-2-ylmethoxyimino)propyl]phenyl}trifluoromethanesulfonamide 207 (364 mg, 85%), as a white solid. M.p. 53-54° C. 1H n.m.r. (400 MHz, CDCl3) δ 11.49, br s,1H; 7.64, d, J=8.8 Hz, 1H; 7.47, d, J=2.4 Hz, 1H; 7.33, m, 2H; 7.16, m, 1H; 7.01, m, 1H; 2.82, q, J=7.6 Hz, 2H; 1.17, t, J=7.6 Hz, 3H. HRMS (M+) 426.0065.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312248B2
Source datasetuspto-grants-2007_12
ORD IDord-f98add91de98481fb39c23f23117a673
Source noteuspto-grants-2007_12