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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970866Generated: October 27, 2026

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

https://huagongshe.com/reaction/970866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant2-(cyclopropylmethoxy)-1H-isoindole-1,3(2H)-dioneHCID 1484310—
ReactantN-(4-chloro-2-propionylphenyl)trifluoromethanesulfonamideHCID 67269822—
SolventEthanolHCID 702—
ProductN-[4-chloro-2-(1-cyclopropylmethoxyiminopropyl)phenyl]trifluoromethanesulfonamideHCID 7303609153.3%

Reaction Steps

N,N-Dimethylethylenediamine (254 μL, 2.20 mmol) was added to a solution of N-(cyclopropylmethoxy)phthalimide (326 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 the addition of a solution of N-(4-chloro-2-propionylphenyl)trifluoromethanesulfonamide 22 (316 mg, 1.0 mmol) in EtOH (2 mL), and the mixture stirred for 65 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-cyclopropylmethoxyiminopropyl)phenyl]trifluoromethanesulfonamide 196 (205 mg, 53%), as a colorless oil. 1H n.m.r. (400 MHz, CDCl3) δ 11.88, br s,1H; 7.66, d, J=8.8 Hz, 1H; 7.49, d, J=2.4 Hz, 1H; 7.33, dd, J=2.4 and 8.8 Hz, 1H; 4.02, d, J=7.2 Hz, 1H; 2.83, q, J=7.6 Hz, 2H; 1.22, m, 4H; 0.64, m, 2H; 0.33, m, 2H. HRMS (M+) 384.0515.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312248B2
Source datasetuspto-grants-2007_12
ORD IDord-7b988fbb2579494fac088b900ed53d04
Source noteuspto-grants-2007_12