Sodium Hydroxide → HCID 3059434, Verbindung

HRID 66908Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 66908
[CH3:1][C:2]([O:6][C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[N:12]([CH2:16][CH2:17][CH3:18])[C:11]([CH3:19])=[C:10]2[C:20]1[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=1)([CH3:5])[CH2:3][OH:4].[OH-].[Na+].[Mn]([O-])(=O)(=O)=[O:29].[K+]>O1CCOCC1.O>[CH3:1][C:2]([O:6][C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[N:12]([CH2:16][CH2:17][CH3:18])[C:11]([CH3:19])=[C:10]2[C:20]1[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=1)([CH3:5])[C:3]([OH:29])=[O:4]

Komponenten

6

Versuchsvorschrift

An amount of 3.38 g (10 m mole) of 2-methyl-2-[2-methyl-1-propyl-3-(4-pyridyl)-1H-indole-5-yloxy]propanol in 50 ml of dioxane was successively mixed with 300 mg of sodium hydroxide in 5 ml of water and then with 3.4 g of potassium permanganate dissolved in 30 ml of water. After stirring for 12 hours, the reaction mixture was filtered, evaporated, and neutralized with dilute sulfuric acid. After extraction with chloroform, the organic phase was dried over sodium sulfate and evaporated. The evaporation residue was recrystallized from ethanol.

Aufarbeitung

  1. filtrationthe reaction mixture was filtered
  2. customevaporated
  3. extractionAfter extraction with chloroform
  4. dry with materialthe organic phase was dried over sodium sulfate
  5. customevaporated
  6. customThe evaporation residue was recrystallized from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-47e4be5935044b9eb9e6ff96489fdc5c
Quelldatensatz
uspto-grants-1982_08
Patentnummer
US04343811

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