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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970855Generated: October 30, 2026

Acetic Acid → N-[4-chloro-2-(1-cyclopentyloxyiminoethyl)phenyl]trifluoromethanesulfonamide

https://huagongshe.com/reaction/970855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant2-(cyclopentyloxy)-1H-isoindole-1,3(2H)-dioneHCID 10263287—
ReactantN-(2-acetyl-4-chlorophenyl)trifluoromethanesulfonamideHCID 67271047—
SolventEthanolHCID 702—
ProductN-[4-chloro-2-(1-cyclopentyloxyiminoethyl)phenyl]trifluoromethanesulfonamideHCID 8660399848.1%

Reaction Steps

N,N-Dimethylethylenediamine (254 μL, 2.20 mmol) was added to a solution of N-(cyclopentyloxy)phthalimide (345 mg, 1.50 mmol) in EtOH (5 mL), and the reaction allowed to stir at RT for 15 h. Glacial acetic acid (2 mL) was then added to adjust the mixture to ca. pH 4 followed by a solution of N-(2-acetyl-4-chlorophenyl)trifluoromethanesulfonamide 19 (302 mg, 1.0 mmol) in EtOH (2 mL), and the reaction stirred for 2.25 h at RT. The reaction mixture was concentrated under vacuum, and the residue purified by radial thin layer chromatography (eluting with CH2Cl2/PE, 1:19) to afford N-[4-chloro-2-(1-cyclopentyloxyiminoethyl)phenyl]trifluoromethanesulfonamide 163 (185 mg, 48%), as a pale yellow solid. 1H n.m.r. (400 MHz, CDCl3) δ 12.18, br s, 1H; 7.67, d, J=8.8 Hz, 1H; 7.49, d, J=2.4 Hz, 1H; 7.31, dd, J=2.4 and 8.8 Hz, 1H; 4.80, m, 1H; 2.30, s, 3H; 1.89, m, 4H; 1.74, m, 2H; 1.64, m, 2H. HRMS (M+) 384.0518.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312248B2
Source datasetuspto-grants-2007_12
ORD IDord-81b927e4f0c54253a3953dc66bb2e759
Source noteuspto-grants-2007_12