Diethyl Oxalate → Ethyl 6-dimethylamino-2,4-dioxo-5-phenyl-5-hexenoate

HRID 1902663Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1902663
[O-]CC.[Na+].[H-].[Na+].[CH3:7][N:8]([CH3:20])[CH:9]=[C:10]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:11](=[O:13])[CH3:12].[C:21](OCC)(=[O:27])[C:22]([O:24][CH2:25][CH3:26])=[O:23]>CCOCC.C(OCC)(=O)C.O.C(O)(=O)C.C(O)C>[CH3:20][N:8]([CH3:7])[CH:9]=[C:10]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:11](=[O:13])[CH2:12][C:21](=[O:27])[C:22]([O:24][CH2:25][CH3:26])=[O:23]

Komponenten

10

Versuchsvorschrift

A suspension of sodium ethoxide was prepared by addition of ethanol (1.6 ml) to a stirred suspension of sodium hydride (1.3 g 50% dispersion, washed with petroleum spirit 40°-60° C.) in ether (50 ml) under nitrogen. A solution of 4-dimethylamino-3-phenyl-3-buten-2-one (4.8 g) and diethyl oxalate (5.2 ml) in ether (50 ml) was added to the stirred sodium ethoxide suspension at 5° to 10° C. and the resulting clear solution was stirred for 2 hours at room temperature, then cooled and treated with glacial acetic acid (2.5 ml) and water (50 ml). Ethyl acetate was added to dissolve the solid which formed and the solvent layer was washed with water, dried, and evaporated. The solid residue was recrystallised from ethyl acetate-petroleum spirit (60°-80° C.) to give ethyl 6-dimethylamino-2,4-dioxo-5-phenyl-5-hexenoate (mp 110° C.).

Aufarbeitung

  1. temperaturecooled
  2. dissolutionto dissolve the solid which
  3. customformed
  4. washthe solvent layer was washed with water
  5. customdried
  6. customevaporated
  7. customThe solid residue was recrystallised from ethyl acetate-petroleum spirit (60°-80° C.)

Quellen und Nachweise

ORD-Eintrag
ord-c5b4261b54e84bae961ddbe894683a3b
Quelldatensatz
uspto-grants-1982_12
Patentnummer
US04364956

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