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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602609Generated: October 25, 2026

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

https://huagongshe.com/reaction/602609

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 numberUS07906538B2
Source datasetuspto-grants-2011_03
ORD IDord-df08ee9f1b9542e6817d307ac7f5edc4
Source noteuspto-grants-2011_03