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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | 2-(2-Thienylmethoxy)-1H-isoindole-1,3(2H)-dione | HCID 10706403 | — |
| Reactant | N-(4-chloro-2-propionylphenyl)trifluoromethanesulfonamide | HCID 67269822 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-{4-chloro-2-[1-(thiophen-2-ylmethoxyimino)propyl]phenyl}trifluoromethanesulfonamide | HCID 86604005 | 85.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906538B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-df08ee9f1b9542e6817d307ac7f5edc4 |
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| Source note | uspto-grants-2011_03 |
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