Reaktion #60216

Reaktionsgleichung

Diethyl (2Z)-3-phenylpent-2-ene-1,5-dioate

NaH

ethyl formate

→

diethyl (3E)-2-(hydroxymethylene)-3-phenylpent-3-ene-1,5-dioate

Ausbeute 97.0%

Lösungsmittel

Et2O

Et2O

Et2O

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturwere refluxed under argon for 15 min
2. 2
   TemperaturThe reaction was heated
3. 3
   Waschenwashed with sat. NH4Cl (40 ml), half sat. NH4Cl (40 ml), brine (20 ml)
4. 4
   Trocknendried with Na2SO4
5. 5
   Filtrationfiltered
6. 6
   Einengenconcentrated under reduced pressure

Vorschrift

A stirred mixture of NaH (158.4 mg, 6.6 mmol) and ethyl formate (1.07 ml, 13.2 mmol) in Et2O (5 ml) were refluxed under argon for 15 min. Diethyl (2Z)-3-phenylpent-2-ene-1,5-dioate in Et2O (5 ml) was added dropwise to the above solution over 5 min at rt. The reaction was heated to retlux for 12 hours. The heterogeneous yellow mixture was diluted with Et2O (100 ml), washed with sat. NH4Cl (40 ml), half sat. NH4Cl (40 ml), brine (20 ml), dried with Na2SO4, filtered, and concentrated under reduced pressure. The product diethyl (3E)-2-(hydroxymethylene)-3-phenylpent-3-ene-1,5-dioate was obtained in 97% yield and could be used without further purification.

Quelle