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Potassium Hydroxide → Ethyl 2-benzylacrylate

HRID 6080
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 6080
[OH-].[K+].[CH2:3]([O:5][C:6](=[O:20])[CH:7]([CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:8](OCC)=O)[CH3:4]>C(O)C>[CH2:3]([O:5][C:6](=[O:20])[C:7]([CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[CH2:8])[CH3:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14797Potassium HydroxideHCID 69090Diethyl 2-benzylpropanedioate

Produkt 1

HCID 11084648Ethyl 2-benzylacrylateAusbeute 85 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel2×

Versuchsvorschrift

A mixture of 4.0 g of KOH in 50 ml of ethanol was added at room temperature to 20 g of benzylmalonic acid diethyl ester in 40 ml of ethanol. The mixture was stirred overnight at room temperature, then concentrated by evaporation, thereafter 7.1 ml of water was added and then the mixture was acidified in an ice bath with 6.3 ml of concentrated hydrochloric acid. Partitioning between water and ether was carried out, the organic phase was dried and the ether was distilled off. Then, 12.9 ml of pyridine, 0.61 g of piperidine and 1.78 g of paraformaldehyde were added to the residue. The mixture was heated in an oil bath (130° ) for 90 minutes, cooled, 220 ml of water was added and extraction was carried out 3 times with 75 ml of n-hexane. The combined organic phases were washed alternatively with water, 1N HCl, water, saturated NaHCO3 solution and brine. The solution was dried (MgSO4) and evaporated to give the title compound as colorless oil (26 g, 85% yield) 1H NMR: 300 MHz; spectrum consistent with proposed structure.

Aufarbeitung

  1. concentrationconcentrated by evaporation
  2. addition7.1 ml of water was added
  3. customthe mixture was acidified in an ice bath with 6.3 ml of concentrated hydrochloric acid
  4. customPartitioning between water and ether
  5. customthe organic phase was dried
  6. distillationthe ether was distilled off
  7. additionThen, 12.9 ml of pyridine, 0.61 g of piperidine and 1.78 g of paraformaldehyde were added to the residue
  8. temperatureThe mixture was heated in an oil bath (130° ) for 90 minutes
  9. temperaturecooled
  10. addition220 ml of water was added
  11. extractionextraction
  12. washThe combined organic phases were washed alternatively with water, 1N HCl, water, saturated NaHCO3 solution and brine
  13. dry with materialThe solution was dried (MgSO4)
  14. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-87cf19ff99b24841930e842d4ab30e9b
Quelldatensatz
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05246969

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