反応 #792146

ord-9224b33b097a4dfc9e90a7776e8d074b

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他to give a yellow solution
  2. 2
    ろ過The reaction mixture was filtered
  3. 3
    その他evaporated
  4. 4
    洗浄the solid residue was washed with diethylether
  5. 5
    その他dried

実験手順

(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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09173424B2uspto-grants-2015_11