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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | 2-(cyclopropylmethoxy)-1H-isoindole-1,3(2H)-dione | HCID 1484310 | — |
| Reactant | N-(4-chloro-2-propionylphenyl)trifluoromethanesulfonamide | HCID 67269822 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[4-chloro-2-(1-cyclopropylmethoxyiminopropyl)phenyl]trifluoromethanesulfonamide | HCID 73036091 | 53.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312248B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-7b988fbb2579494fac088b900ed53d04 |
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| Source note | uspto-grants-2007_12 |
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