Acetanilide → N-[4-(3,4-Dinitrobenzoyl)phenyl]acetamide

HRID 1294077Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1294077
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[N+:13]([O-:15])=[O:14])[C:7](Cl)=[O:8])([O-:3])=[O:2].[C:16]([NH:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)(=[O:18])[CH3:17].[Al+3].[Cl-].[Cl-].[Cl-]>C(Cl)Cl>[C:16]([NH:19][C:20]1[CH:25]=[CH:24][C:23]([C:7]([C:6]2[CH:10]=[CH:11][C:12]([N+:13]([O-:15])=[O:14])=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)=[O:8])=[CH:22][CH:21]=1)(=[O:18])[CH3:17]

Komponenten

5

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

A mixture of 3,4-dinitrobenzoyl chloride (4 mmol), acetoanilide (540 mg, 4 mmol), and AlCl3 (1.6 g) in CH2Cl2 was heated at 40° C. for 24 h. The slurry was washed with HCl (aq) and the product was extracted with ether. It was washed with K2CO3 (aq), dried, and evaporated. Purification by column-chromatography on silica-gel (hexane:AcOEt=1:3) provided 87 mg of the title compound; MS m/e 328 (M−1).

Aufarbeitung

  1. washThe slurry was washed with HCl (aq)
  2. extractionthe product was extracted with ether
  3. washIt was washed with K2CO3 (aq)
  4. customdried
  5. customevaporated
  6. customPurification by column-chromatography on silica-gel (hexane:AcOEt=1:3)

Quellen und Nachweise

ORD-Eintrag
ord-4349b20b0a53459590cf7676c88ddd05
Quelldatensatz
uspto-grants-2007_07
Patentnummer
US07238813B2

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