Ethyl Acetoacetate → Ethyl 2-acetyl-5-chlorohex-4-enoate

HRID 437927

Reaktionsgleichung

Reaktionsgleichung von HRID 437927
[Na].[C:2]([O:8][CH2:9][CH3:10])(=[O:7])[CH2:3][C:4]([CH3:6])=[O:5].Cl[CH2:12][CH:13]=[C:14]([Cl:16])[CH3:15]>C(O)C>[C:2]([CH:3]([CH2:12][CH:13]=[C:14]([Cl:16])[CH3:15])[C:4](=[O:5])[CH3:6])([O:8][CH2:9][CH3:10])=[O:7]

Komponenten

5

Edukt 3

HCID 8868Ethyl AcetoacetateHCID 135561,3-Dichloro-2-buteneHCID 5360545Sodium

Produkt 1

HCID 53723570Ethyl 2-acetyl-5-chlorohex-4-enoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

To a solution of 46 g sodium (2 g atom) in 500 ml ethanol at reflux, in a 2-liter flask equipped with mechanical stirrer, and addition funnel, was added 325 g ethyl acetoacetate (2.5 mole) over 30 minutes. The resulting solution of enolate was refluxed for 15 minutes, and then 250 g (2.0 mole) 1,3-dichlorobut-2-ene was added dropwise at such a rate as to maintain reflux with gentle heating towards the end of the addition. After addition, refluxing and stirring were maintained for 4 hours, the condenser converted for distillation, and ethanol removed as 500 ml distillate. The residual product was cooled, water and 1.2 N hydrochloric acid were added and the organic layer separated. The aqueous portion was extracted with ether, the organic layers combined, washed with water and brine, filtered through sodium sulfate and evaporated in vacuo to give 485 g dark yellow oil (96%, based on dichlorobutene). Vpc showed 73% of trans plus cis product, together with other volatiles.

Aufarbeitung

  1. customequipped with mechanical stirrer, and addition funnel
  2. temperatureto maintain
  3. temperaturereflux
  4. temperaturewith gentle heating towards the end of the addition
  5. additionAfter addition
  6. temperaturerefluxing
  7. temperaturewere maintained for 4 hours
  8. distillationthe condenser converted for distillation, and ethanol
  9. customremoved as 500 ml distillate
  10. temperatureThe residual product was cooled
  11. additionwater and 1.2 N hydrochloric acid were added
  12. customthe organic layer separated
  13. extractionThe aqueous portion was extracted with ether
  14. washwashed with water and brine
  15. filtrationfiltered through sodium sulfate
  16. customevaporated in vacuo
  17. customto give 485 g dark yellow oil (96%, based on dichlorobutene)

Quellen und Nachweise

ORD-Eintrag
ord-11bdc12696714030955907e82a987942
Quelldatensatz
uspto-grants-1977_06
Patentnummer
US04032579

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