Reaktion #343727

Reaktionsgleichung

diethyl acetamidomalonate

2,3-dibromopropene

sodium hydride

→

desired product

Ausbeute 89.5%

Diethyl (2-Bromoallyl)acetamidomalonate

Ausbeute 89.5%

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturheated to reflux
2. 2
   TemperaturAfter heating for 18 h
3. 3
   Temperaturthe resultant slurry was cooled to room temperature
4. 4
   Filtrationsuction filtered through a short pad of silica gel
5. 5
   WaschenThe solid residue was washed with tetrahydrofuran (2×50 mL)
6. 6
   Einengenconcentrated
7. 7
   workup.DISSOLUTIONThe residue was dissolved in ethyl acetate (2.0 L)
8. 8
   Waschenwashed with water and brine
9. 9
   Trocknenwas dried over MgSO4
10. 10
    FiltrationFiltration and concentration
11. 11
    Sonstigegave a yellow oil which
12. 12
    Sonstigeupon drying
13. 13
    SonstigeThe resultant solid was recrystallized from a mixture of hot ethyl acetate/hexane

Vorschrift

To a stirred mixture of diethyl acetamidomalonate (217 g, 1.0 mol) and 2,3-dibromopropene (240 g, 1.2 mol) in dry tetrahydrofuran (2.50 L), under nitrogen, was added sodium hydride (26.4 g, 1.1 mol) in several portions. The reaction mixture was stirred at room temperature for 30 min, then heated to reflux. After heating for 18 h, the resultant slurry was cooled to room temperature and suction filtered through a short pad of silica gel. The solid residue was washed with tetrahydrofuran (2×50 mL), and the filtrates were combined and concentrated. The residue was dissolved in ethyl acetate (2.0 L), washed with water and brine, and then was dried over MgSO4. Filtration and concentration gave a yellow oil which solidified upon drying. The resultant solid was recrystallized from a mixture of hot ethyl acetate/hexane to give 301 g (89%) of the desired product: m.p. 85°-87° C.

Quelle