1-(Hydroxymethyl)isoquinoline → Isoquinoline-1-carbaldehyde

HRID 348659

Reaktionsgleichung

Reaktionsgleichung von HRID 348659
[C:1]1([CH2:11][OH:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N:2]=1>C(Cl)(Cl)Cl.[O-2].[O-2].[Mn+4]>[C:1]1([CH:11]=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N:2]=1

Komponenten

4

Versuchsvorschrift

Isoquinolin-1-yl-methanol (123.7 mg) was dissolved in chloroform (6.2 ml) and then added with manganese dioxide (chemically processed product) (1.24 g), followed by stirring at room temperature for 30 minutes. The reaction solution was filtrated through Celite and the solvent was then distilled off. The residue was dried under vacuum, thereby obtaining the subject compound (103.9 mg) as a brown solid.

Aufarbeitung

  1. filtrationThe reaction solution was filtrated through Celite
  2. distillationthe solvent was then distilled off
  3. customThe residue was dried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-08bcf8622f984d33a60644c8f0c66571
Quelldatensatz
uspto-grants-2007_02
Patentnummer
US07176227B2

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