3-Methyl-2,3,4,5,6,7-hexahydro-1H-inden-1-one → 1,3-dimethyl-4,5,6,7-tetrahydro-1H-indene

HRID 863389Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 863389
[CH3:1][Li].[CH3:3][CH:4]1[C:12]2[CH2:11][CH2:10][CH2:9][CH2:8][C:7]=2[C:6](=O)[CH2:5]1>C(OCC)C>[CH3:3][C:4]1[C:12]2[CH2:11][CH2:10][CH2:9][CH2:8][C:7]=2[CH:6]([CH3:1])[CH:5]=1

Komponenten

4

Edukt 2

HCID 111055313-Methyl-2,3,4,5,6,7-hexahydro-1H-inden-1-oneHCID 178418348HCID 178418348, Verbindung

Produkt 1

HCID 129801691,3-dimethyl-4,5,6,7-tetrahydro-1H-indeneAusbeute 45 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

Methyl lithium (1.5M, 96 ml) was added dropwise to a solution of 4,5,6,7-tetrahydro-1-methyl-indan-3-one (17.7 g, 0.118 mol) in 50 ml of diethyl ether under an argon atmosphere whereupon the reaction mixture was refluxed for 18 hours. The mixture after this time period was hydrolyzed and the reaction mixture extracted with diethyl ether. The ether extracts were dried over anhydrous MgSO4 and filtered. To the ether solution, 0.5 ml of 6M HCl was added and the solution stirred for one hour. After this time period the ether solution was washed with water, dried over anhydrous MgSO4, filtered and concentrated. Distillation at reduced pressure afforded 8.0 g (45 percent) of product.

Aufarbeitung

  1. temperaturewas refluxed for 18 hours
  2. extractionthe reaction mixture extracted with diethyl ether
  3. dry with materialThe ether extracts were dried over anhydrous MgSO4
  4. filtrationfiltered
  5. additionTo the ether solution, 0.5 ml of 6M HCl was added
  6. washAfter this time period the ether solution was washed with water
  7. dry with materialdried over anhydrous MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. distillationDistillation at reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-313b6a4f8ac54c16820fa8a66479cbeb
Quelldatensatz
uspto-grants-1998_02
Patentnummer
US05721185

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