Allyl chloride → N-Allyl-N-(1,1-dimethoxyprop-2-yl)-urethane

HRID 974914

Reaktionsgleichung

Reaktionsgleichung von HRID 974914
[CH3:1][O:2][CH:3]([O:12][CH3:13])[CH:4]([NH:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH3:5].[H-].[Na+].[H][H].[CH2:18](Cl)[CH:19]=[CH2:20]>C1(C)C=CC=CC=1>[CH2:20]([N:6]([CH:4]([CH3:5])[CH:3]([O:2][CH3:1])[O:12][CH3:13])[C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH:19]=[CH2:18]

Komponenten

6

Edukt 4

HCID 7850Allyl chlorideHCID 24758Sodium hydrideHCID 15069987N-(1,1-dimethoxyprop-2-yl)urethaneHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 15069988N-Allyl-N-(1,1-dimethoxyprop-2-yl)-urethane

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

131 g (0.686 mol) of N-(1,1-dimethoxyprop-2-yl)-urethane are added dropwise to 25 g of sodium hydride (80% strength) in 700 ml of absolute toluene at 90° C. When the evolution of hydrogen has ended, 61.2 g (0.8 mol) of allyl chloride are added dropwise at 90° C. and the mixture is stirred overnight at 90° C. The sodium chloride which has precipitated out is dissolved with water, the organic phase is separated off, dried over K2CO3 and concentrated and the residue is distilled.

Aufarbeitung

  1. customThe sodium chloride which has precipitated out
  2. dissolutionis dissolved with water
  3. customthe organic phase is separated off
  4. dry with materialdried over K2CO3
  5. concentrationconcentrated
  6. distillationthe residue is distilled

Quellen und Nachweise

ORD-Eintrag
ord-fae9625609f04569bd5317e869caf537
Quelldatensatz
uspto-grants-1997_03
Patentnummer
US05607942

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