3,5-Dimethyl-4-hydroxybenzaldehyde → HCID 66704300, Verbindung

HRID 132083

Reaktionsgleichung

Reaktionsgleichung von HRID 132083
CCCC(O[CH2:8][C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:10])CC.[CH3:17][C:18]1[CH:19]=[C:20]([CH:23]=[C:24]([CH3:27])[C:25]=1[OH:26])[CH:21]=O>>[CH2:9]([O:10][C:14]1[CH:13]=[CH:12][C:11]([C:9](=[O:10])[CH:8]=[CH:21][C:20]2[CH:19]=[C:18]([CH3:17])[C:25]([OH:26])=[C:24]([CH3:27])[CH:23]=2)=[CH:16][CH:15]=1)[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15]

Komponenten

3

Edukt 2

HCID 752223,5-Dimethyl-4-hydroxybenzaldehydeHCID 53842574HCID 53842574, Verbindung

Produkt 1

HCID 66704300HCID 66704300, VerbindungAusbeute 63 %

Versuchsvorschrift

This compound was synthesized from 4-hexyloxyacetophenone and 3,5-dimethyl-4-hydroxybenzaldehyde according to general method 1 described hereinabove. The product crystallized at the end of the reaction and was dried. Yield: 63%

Aufarbeitung

  1. customThe product crystallized at the end of the reaction
  2. customwas dried

Quellen und Nachweise

ORD-Eintrag
ord-8a666137ddbb47e6b229b3ccd4636024
Quelldatensatz
uspto-grants-2008_06
Patentnummer
US07385082B2

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