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Ethyl 3-(dimethoxymethyl)-crotonate → Ethyl 3-methyl-4-oxobutanoate

HRID 1650775
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1650775
C[O:2][CH:3](OC)/[C:4](/[CH3:11])=[CH:5]\[C:6]([O:8][CH2:9][CH3:10])=[O:7]>C(OCC)(=O)C.[Pd]>[CH:3]([CH:4]([CH3:11])[CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 13405211Ethyl 3-(dimethoxymethyl)-crotonate

Produkt 1

HCID 13000833Ethyl 3-methyl-4-oxobutanoateAusbeute 48 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A solution of ethyl 3-(dimethoxymethyl)-crotonate (73 g) in ethyl acetate (200 ml) was hydrogenated at 50 psi for 3 h in the presence of 10% palladium on charcoal (7 g). The solution was filtered, evaporated, and the residual oil treated with 0.25 M hydrogen chloride in 75% aqueous methanol for 2 h. To the reaction mixture was added ethyl acetate (300 ml) and water (150 ml). The organic phase was successively washed with sat. sodium bicarbonate solution (3×150 ml), water (100 ml) and dried over magnesium sulfate. The solution was concentrated in vacuo and the residual oil purified by chromatography on silica gel eluting with ethyl acetate-hexane (1:9) to give ethyl 3-formylbutyrate (26.5 g, 48%).

Aufarbeitung

  1. filtrationThe solution was filtered
  2. customevaporated
  3. additionthe residual oil treated with 0.25 M hydrogen chloride in 75% aqueous methanol for 2 h
  4. additionTo the reaction mixture was added ethyl acetate (300 ml) and water (150 ml)
  5. washThe organic phase was successively washed with sat. sodium bicarbonate solution (3×150 ml), water (100 ml)
  6. dry with materialdried over magnesium sulfate
  7. concentrationThe solution was concentrated in vacuo
  8. customthe residual oil purified by chromatography on silica gel eluting with ethyl acetate-hexane (1:9)

Quellen und Nachweise

ORD-Eintrag
ord-19a7fd19968544d489a087e687ecdcb8
Quelldatensatz
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04925867

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