methyl (2E)-3-(pyrimidin-5-yl)prop-2-enoate → Methyl 3-(pyrimidin-5-yl)propanoate

HRID 474543Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 474543
[N:1]1[CH:6]=[C:5](/[CH:7]=[CH:8]/[C:9]([O:11][CH3:12])=[O:10])[CH:4]=[N:3][CH:2]=1>CO.[Pd]>[N:1]1[CH:6]=[C:5]([CH2:7][CH2:8][C:9]([O:11][CH3:12])=[O:10])[CH:4]=[N:3][CH:2]=1

Komponenten

4

Versuchsvorschrift

A solution of methyl (2E)-3-(5-pyrimidinyl)-2-propenoate (19.2 g, 117 mmol) and Pd/C (2 g, 1.879 mmol) in methanol (100 mL) was stirred under H2 at 50° C. overnight. The mixture was filtered through a pad of celite and concentrated to give the crude title compound as yellow oil (18 g, 55.6% yield). LCMS: rt=1.11 min, [M+H+]=167

Aufarbeitung

  1. filtrationThe mixture was filtered through a pad of celite
  2. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-c77d9593e92e4cfab70f3c89c785d9fe
Quelldatensatz
uspto-grants-2014_01
Patentnummer
US08637536B2

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