7-Quinolinemethanol → 7-Quinolinecarboxaldehyde

HRID 1756509

Reaktionsgleichung

Reaktionsgleichung von HRID 1756509
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([CH2:11][OH:12])[CH:9]=2)[CH:4]=[CH:3][CH:2]=1>[O-2].[Mn+4].[O-2].ClCCl>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([CH:11]=[O:12])[CH:9]=2)[CH:4]=[CH:3][CH:2]=1

Komponenten

4

Edukt 1

HCID 976097-Quinolinemethanol

Produkt 1

HCID 47122557-QuinolinecarboxaldehydeAusbeute 94,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178418406HCID 178418406, VerbindungKatalysatorHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A mixture of 8.6 parts of 7-quinolinemethanol, 20 parts of manganese(IV)oxide and 130 parts of dichloromethane was stirred for 24 hours at room temperature. The reaction mixture was filtered over diatomaceous earth and the filtrate was evaporated. The residue was purified by column chromatography (silica gel; CH2Cl2 /CH3OH 98:2). The eluent of the desired fraction was evaporated, yielding 8 parts (94.2%) of 7-quinolinecarboxaldehyde; mp. 56° C. (interm. 1).

Aufarbeitung

  1. filtrationThe reaction mixture was filtered over diatomaceous earth
  2. customthe filtrate was evaporated
  3. customThe residue was purified by column chromatography (silica gel; CH2Cl2 /CH3OH 98:2)
  4. customThe eluent of the desired fraction was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-7436c58ac20b4d8eaa166d96b056357c
Quelldatensatz
uspto-grants-1995_08
Patentnummer
US05441954

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