Reaktion #462758

ord-745dc2ab3062421ab362e02db49ab10b

Reaktionsgleichung

O=C(O)Cc1ccc2c(c1)OCO2
3,4-Methylenedioxyphenylacetic acid
[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminium hydride
OCCc1ccc2c(c1)OCO2
title compound
Ausbeute 90.4%
OCCc1ccc2c(c1)OCO2
3,4-Methylenedioxyphenethyl alcohol
Ausbeute 90.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled
  2. 2
    Sonstigequenched by the cautious addition of saturated aqueous ammonium chloride solution
  3. 3
    Filtrationfiltered
  4. 4
    WaschenThe filtrate was washed with 10% aqueous sodium carbonate solution
  5. 5
    Trocknendried over magnesium sulphate
  6. 6
    Sonstigeevaporated

Vorschrift

3,4-Methylenedioxyphenylacetic acid (18.0 g) was added portionwise over 30 minutes to a stirred, ice-cooled suspension of lithium aluminium hydride (4.0 g) in ether (400 ml) and the mixture was stirred at room temperature for two hours, quenched by the cautious addition of saturated aqueous ammonium chloride solution and filtered. The filtrate was washed with 10% aqueous sodium carbonate solution, dried over magnesium sulphate and evaporated to give the title compound as a pale yellow oil (15.01 g, 90%), which was characterised by its 1H-NMR spectrum.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05486527uspto-grants-1996_01