Reaktion #792146

ord-9224b33b097a4dfc9e90a7776e8d074b

Reaktionsgleichung

O=C(/C=C/c1ccccn1)c1ccc2c(c1O)OCO2
(E)-1-(4-hydroxybenzo[d][1,3]dioxol-5-yl)-3-(pyridin-2-yl)prop-2-en-1-one
O=C(CCc1ccccn1)c1ccc2c(c1O)OCO2
title compound
Ausbeute 59.6%
O=C(CCc1ccccn1)c1ccc2c(c1O)OCO2
1-(4-hydroxybenzo[d][1,3]dioxol-5-yl)-3-(pyridin-2-yl)propan-1-one
Ausbeute 59.6%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto give a yellow solution
  2. 2
    FiltrationThe reaction mixture was filtered
  3. 3
    Sonstigeevaporated
  4. 4
    Waschenthe solid residue was washed with diethylether
  5. 5
    Sonstigedried

Vorschrift

(E)-1-(4-hydroxybenzo[d][1,3]dioxol-5-yl)-3-(pyridin-2-yl)prop-2-en-1-one (0.5 g, 1.857 mmol) was added to methanol (50 ml) to give a yellow solution. Palladium on carbon (0.05 g) was added. Product was hydrogenated while stirring till conversion was completed (checked by TLC). The reaction mixture was filtered, evaporated and the solid residue was washed with diethylether, and dried to yield 0.3 g (57%) of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09173424B2uspto-grants-2015_11