Reaktion #3498

ord-cf112f9f981e4357be02e4ddbd112b54

Reaktionsgleichung

O
water
[H-].[Na+]
sodium hydride
CONC(=O)OC
methyl N-methoxycarbamate
C#CCBr
propargyl bromide
C#CCN(OC)C(=O)OC
methyl N-methoxy-N-propargylcarbamate
Ausbeute 58.7%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhile being cooled with ice
  2. 2
    TemperaturThe mixture was heat-refluxed for 4 hours
  3. 3
    workup.ADDITIONwas added to the reaction solution
  4. 4
    Extraktionthe mixture was extracted with ethyl acetate
  5. 5
    SonstigeThe extract was dried
  6. 6
    Einengenconcentrated
  7. 7
    Sonstigepurified by silica gel column chromatography

Vorschrift

0.43 g of sodium hydride (60% in oil) was suspended in 10 ml of tetrahydrofuran, and 1.0 g of methyl N-methoxycarbamate and 1.36 g of propargyl bromide were added to the suspension in this order while being cooled with ice. The mixture was heat-refluxed for 4 hours. After completion of the reaction, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was dried, concentrated and purified by silica gel column chromatography to obtain 0.8 g of methyl N-methoxy-N-propargylcarbamate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05733935uspto-grants-1998_03