Water → Ethyl (4Z)-8-oxo-4-octenoate

HRID 1729784Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1729784
[OH:1][CH:2]1[CH2:9][CH2:8][CH:7]=[CH:6][CH2:5][CH2:4][C:3]1=[O:10].[CH2:11](O)[CH3:12].C1C=CC=CC=1.C([O-])(=[O:22])C.C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C.[Pb+4].O>CCOCC>[O:10]=[CH:3][CH2:4][CH2:5]/[CH:6]=[CH:7]\[CH2:8][CH2:9][C:2]([O:1][CH2:11][CH3:12])=[O:22]

Komponenten

6

Edukt 4

HCID 962WaterHCID 2737052-Hydroxy-5-cycloocten-1-oneHCID 21965192Npc112006HCID 178418268HCID 178418268, Verbindung

Produkt 1

HCID 24972431Ethyl (4Z)-8-oxo-4-octenoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

To 220 mg. of 2-hydroxy-5-cycloocten-1-one in 5 ml. of 30% ethanol/benzene is added 860 mg. of 85% lead tetraacetate in portions. After about 3 hours at room temperature, water and ether are added to the reaction mixture. The aqueous phase is extracted several times with ether. The combined ether extracts are washed with 2M sodium carbonate and saturated sodium chloride solution, dried over calcium sulfate and evaporated to give ethyl (4Z)-8-oxo-4-octenoate in high purity.

Aufarbeitung

  1. extractionThe aqueous phase is extracted several times with ether
  2. washThe combined ether extracts are washed with 2M sodium carbonate and saturated sodium chloride solution
  3. dry with materialdried over calcium sulfate
  4. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-f61c5352f25946a28d95230fc3da0343
Quelldatensatz
uspto-grants-1976_11
Patentnummer
US03989729

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