2-Hydroxy-3,4,6-trimethylbenzaldehyde → 2,3,5,6-Tetramethylphenol

HRID 15631

Reaktionsgleichung

Reaktionsgleichung von HRID 15631
[OH:1][C:2]1[C:9]([CH3:10])=[C:8]([CH3:11])[CH:7]=[C:6]([CH3:12])[C:3]=1[CH:4]=O>CO.[C].[Pd]>[CH3:4][C:3]1[C:6]([CH3:12])=[CH:7][C:8]([CH3:11])=[C:9]([CH3:10])[C:2]=1[OH:1]

Komponenten

4

Edukt 1

HCID 113211462-Hydroxy-3,4,6-trimethylbenzaldehyde

Produkt 1

HCID 106942,3,5,6-TetramethylphenolAusbeute 12,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178418390HCID 178418390, VerbindungKatalysatorHCID 887MethanolLösungsmittel

Versuchsvorschrift

2-Hydroxy-3,4,6-trimethylbenzaldehyde (6.58 g, 40.1 mmol) was dissolved in methanol (120 mL), 10% palladium-carbon (50% water-containing product, 1.0 g) was added under hydrogen atmosphere (balloon pressure), and the mixture was stirred at room temperature for 22 hr. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The precipitated crystals were recrystallized from methanol to give the title compound (0.73 g, yield 12%) as colorless crystals. The mother solution was concentrated under reduced pressure to give second crop (5.10 g, yield 85%).

Aufarbeitung

  1. filtrationThe catalyst was filtered off
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customThe precipitated crystals were recrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-c8ef37b0098c486e9cda2210405040db
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07732626B2

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