Tert-Butylamine → 3-(t-Butyl-amino)-N-methoxy-N-methyl-propanamide

HRID 915218Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 915218
[CH3:1][O:2][N:3]([CH3:8])[C:4](=[O:7])[CH:5]=[CH2:6].[C:9]([NH2:13])([CH3:12])([CH3:11])[CH3:10]>>[C:9]([NH:13][CH2:6][CH2:5][C:4]([N:3]([O:2][CH3:1])[CH3:8])=[O:7])([CH3:12])([CH3:11])[CH3:10]

Komponenten

3

Versuchsvorschrift

N-Methoxy-N-methyl-acrylamide (5 g, 43.4 mmol, 1.0 equiv) was dissolved in t-butylamine (3.36 g, 46 mmol, 1.06 equiv). The resulting solution was stirred at room temperature for 48 h. The excess primary amine was removed in vacuo and the crude product was purified by flash chromatography on silica using 100% CH2Cl2 to 2% MeOH in CH2Cl2 to give the desired product as a light yellow oil (5.7 g, 70%); MS, m/z 189=M+1.

Aufarbeitung

  1. customThe excess primary amine was removed in vacuo
  2. customthe crude product was purified by flash chromatography on silica using 100% CH2Cl2 to 2% MeOH in CH2Cl2

Quellen und Nachweise

ORD-Eintrag
ord-f99d5ad2b7d14b348d03979b1b694811
Quelldatensatz
uspto-grants-2007_09
Patentnummer
US07265132B2

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