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Methyl 3-acetoxy-2-methylenebutyrate → methyl 2-[(1R)-1-hydroxyethyl]acrylate

HRID 2255657
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2255657
C([O:4][CH:5]([C:7](=[CH2:12])[C:8]([O:10][CH3:11])=[O:9])[CH3:6])(=O)C>P([O-])([O-])([O-])=O>[OH:4][C@@H:5]([C:7](=[CH2:12])[C:8]([O:10][CH3:11])=[O:9])[CH3:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 5102926Methyl 3-acetoxy-2-methylenebutyrate

Produkt 1

HCID 11147730methyl 2-[(1R)-1-hydroxyethyl]acrylateAusbeute 17 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1061PhosphateLösungsmittel

Versuchsvorschrift

A mixture of methyl 2-(1-acetoxyethyl)acrylate (5 g) and "Lipase P" (Trademark; origin : Pseudomonas sp.; maker : Amano Pharmaceutical Co.) (1.25 g) in phosphate buffer solution (0.1M) pH 7.0 (400 ml) was stirred at room temperature for 55 hours. The whole mixture was extracted with ethyl acetate three times and the combined extracts were dried. After removal at the solvent in vacuo, the crude product was purified by column chromatography on silica gel (eluent : a mixture of hexane and ethyl acetate, 2:1). The resultant oily residue (840 mg) was distilled in vacuo to give methyl 2-[(1R)-1-hydroxyethyl]acrylate (644 mg).

Aufarbeitung

  1. extractionThe whole mixture was extracted with ethyl acetate three times
  2. customthe combined extracts were dried
  3. customAfter removal at the solvent in vacuo
  4. customthe crude product was purified by column chromatography on silica gel (eluent
  5. additiona mixture of hexane and ethyl acetate, 2:1)
  6. distillationThe resultant oily residue (840 mg) was distilled in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d60e93df26ee4f8cba1e06dec8077cef
Quelldatensatz
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05241064

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