تفاعل #792146

ord-9224b33b097a4dfc9e90a7776e8d074b

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىto give a yellow solution
  2. 2
    ترشيحThe reaction mixture was filtered
  3. 3
    أخرىevaporated
  4. 4
    غسيلthe solid residue was washed with diethylether
  5. 5
    أخرىdried

الإجراء التجريبي

(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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09173424B2uspto-grants-2015_11