Реакция #792146

ord-9224b33b097a4dfc9e90a7776e8d074b

Уравнение реакции

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
Выход 59.6%
O=C(CCc1ccccn1)c1ccc2c(c1O)OCO2
1-(4-hydroxybenzo[d][1,3]dioxol-5-yl)-3-(pyridin-2-yl)propan-1-one
Выход 59.6%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеto give a yellow solution
  2. 2
    ФильтрацияThe reaction mixture was filtered
  3. 3
    Другоеevaporated
  4. 4
    Промывкаthe solid residue was washed with diethylether
  5. 5
    Другоеdried

Методика

(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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09173424B2uspto-grants-2015_11