Ethanol → Diethyl 2-(2,4-dichlorophenyl)malonate

HRID 1682460Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1682460
[Na].C(O)C.[Cl:5][C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][C:7]=1[CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15].[C:19](=O)([O:23]CC)[O:20][CH2:21][CH3:22]>>[CH3:18][CH2:17][O:16][C:14]([CH:13]([C:19]([O:20][CH2:21][CH3:22])=[O:23])[C:7]1[CH:8]=[CH:9][C:10]([Cl:12])=[CH:11][C:6]=1[Cl:5])=[O:15]

Komponenten

5

Edukt 4

HCID 702Ethanol2×HCID 7766Diethyl CarbonateHCID 234291Ethyl (2,4-dichlorophenyl)acetateHCID 5360545Sodium2×

Produkt 1

HCID 2736112Diethyl 2-(2,4-dichlorophenyl)malonateAusbeute 85 %

Versuchsvorschrift

Sodium (1.86 g, 0.081M) was added in portions to absolute ethanol (150 ml) with stirring. After all the sodium had dissolved a solution of ethyl 2,4-dichlorophenylacetate (20 g) in diethyl carbonate (50 ml) was added dropwise. The reaction mixture was heated until EtOH distilled over. The rate of addition was controlled such that it equalled the rate of distillation. After the completion of addition the reaction mixture was heated and distilled for further 4 hours. The cooled reaction mixture was partitioned between water (300 ml) and EtOAc (300 ml) and the organic layer dried and evaporated in vacuo to give a yellow oil (21 g, 85%).

Aufarbeitung

  1. additionwas added dropwise
  2. distillationdistilled over
  3. additionThe rate of addition
  4. distillationthe rate of distillation
  5. additionAfter the completion of addition the reaction mixture
  6. temperaturewas heated
  7. distillationdistilled for further 4 hours
  8. customThe cooled reaction mixture
  9. customwas partitioned between water (300 ml) and EtOAc (300 ml)
  10. customthe organic layer dried
  11. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-b24f995b55ba4a048687a8789ee61afa
Quelldatensatz
uspto-grants-1997_06
Patentnummer
US05635507

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