Methanol → 3-Methoxy-1,2,4,5-tetramethylbenzene

HRID 1154145

Reaktionsgleichung

Reaktionsgleichung von HRID 1154145
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([CH3:9])=[C:4]([CH3:10])[C:3]=1[OH:11].[CH3:12]I.[H-].[Na+].CO>CS(C)=O.CCOCC.O>[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([CH3:9])=[C:4]([CH3:10])[C:3]=1[O:11][CH3:12]

Komponenten

8

Edukt 4

HCID 887MethanolHCID 6328Methyl iodideHCID 106942,3,5,6-TetramethylphenolHCID 24758Sodium hydride2×

Produkt 1

HCID 2786643-Methoxy-1,2,4,5-tetramethylbenzene

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 679Dimethyl SulfoxideLösungsmittelHCID 962WaterLösungsmittelHCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

In 150 ml of DMSO were dissolved 15.0 g of 2,3,5,6-tetramethylphenol and 28 ml of methyl iodide. Under ice-cooling 6.3 g of 60% sodium hydride in oil was added, and the mixture was stirred at room temperature for 1 hour. The excess sodium hydride was decomposed with MeOH and after addition of water extraction with ether was carried out. The extract was dried over sodium sulfate. Removal of the solvent by distillation leaves crystals which were recrystallized from MeOH.

Aufarbeitung

  1. additionwas added
  2. dry with materialThe extract was dried over sodium sulfate
  3. customRemoval of the solvent
  4. distillationby distillation
  5. customleaves crystals which
  6. customwere recrystallized from MeOH

Quellen und Nachweise

ORD-Eintrag
ord-0a4de214a9c74319ae3e4661470ba931
Quelldatensatz
uspto-grants-1984_12
Patentnummer
US04487726

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