(3,5-Dibromo-4-methoxyphenyl)acetylchloride → 2-(3,5-dibromo-4-methoxy-phenyl)-N-[2-(3-nitro-phenyl)-ethyl]-acetamide

HRID 1358473Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1358473
C(O)(=O)C(O)=O.[N+:7]([C:10]1[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=1)[CH2:13][CH2:14][NH2:15])([O-:9])=[O:8].[Br:19][C:20]1[CH:21]=[C:22]([CH2:29][C:30](Cl)=[O:31])[CH:23]=[C:24]([Br:28])[C:25]=1[O:26][CH3:27]>C(Cl)Cl.[OH-].[Na+]>[Br:19][C:20]1[CH:21]=[C:22]([CH2:29][C:30]([NH:15][CH2:14][CH2:13][C:12]2[CH:16]=[CH:17][CH:18]=[C:10]([N+:7]([O-:9])=[O:8])[CH:11]=2)=[O:31])[CH:23]=[C:24]([Br:28])[C:25]=1[O:26][CH3:27]

Komponenten

5

Versuchsvorschrift

To a suspension of 3-nitro-phenethylamine oxalate (1.792 g, 0.007 mol) in methylene chloride (45 mL), 1 N NaOH (45 mL) was added. It was stirred at room temperature to get a clear solution. A solution of 3,5-dibromo-4-methoxyphenyl acetyl chloride (0.0072 mol) in methylene chloride was added. Stirring was continued overnight and the completion of the reaction was monitored by thin layer chromatography. The reaction mixture was washed with 1N HCl and 1N NaOH, extracted with methylene chloride. The combined extracts were dried over anhydrous sodium sulfate and concentrated. The solid obtained was crystallized from ethyl acetate-hexanes mixture. Yield 2.159 g, 65%.

Aufarbeitung

  1. additionwas added
  2. customto get a clear solution
  3. stirringStirring
  4. washThe reaction mixture was washed with 1N HCl and 1N NaOH
  5. extractionextracted with methylene chloride
  6. dry with materialThe combined extracts were dried over anhydrous sodium sulfate
  7. concentrationconcentrated
  8. customThe solid obtained
  9. customwas crystallized from ethyl acetate-hexanes mixture

Quellen und Nachweise

ORD-Eintrag
ord-0f62632f3260459692aad07ca5f7b1d9
Quelldatensatz
uspto-grants-2003_07
Patentnummer
US06596734B1

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