Acetone → 3-Buten-2-one, 4-(2,3-dihydro-1H-inden-5-yl)-

HRID 1710260Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1710260
[OH-].[Na+].[CH2:3]1[C:11]2[C:6](=[CH:7][C:8]([CH:12]=O)=[CH:9][CH:10]=2)[CH2:5][CH2:4]1.[CH3:14][C:15]([CH3:17])=[O:16]>O>[CH2:3]1[C:11]2[C:6](=[CH:7][C:8]([CH:12]=[CH:14][C:15](=[O:16])[CH3:17])=[CH:9][CH:10]=2)[CH2:5][CH2:4]1

Komponenten

5

Edukt 3

HCID 180AcetoneHCID 14798Sodium HydroxideHCID 1216245-Indanecarboxaldehyde

Produkt 1

HCID 40739273-Buten-2-one, 4-(2,3-dihydro-1H-inden-5-yl)-Ausbeute 81 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

An aqueous solution of 10% sodium hydroxide (50-70 ml) was added dropwise over a period of 5 minutes to a suspension of indane-5-carboxaldehyde (18.50 g; 127 mmole) in acetone (50 ml) and water (50 ml). The mixture was stirred at a temperature of 65° C. for a period of 11/2 hours and then extracted with dichloromethane (200 ml). The organic extract was washed several times with water, dried over anhydrous sodium sulphate, and the solvent was removed under reduced pressure using a rotary evaporator to give 1-(5-indanyl)but-1-en-3-one (19.25 g; 81%) as a viscous oil.

Aufarbeitung

  1. extractionextracted with dichloromethane (200 ml)
  2. extractionThe organic extract
  3. washwas washed several times with water
  4. dry with materialdried over anhydrous sodium sulphate
  5. customthe solvent was removed under reduced pressure
  6. customa rotary evaporator

Quellen und Nachweise

ORD-Eintrag
ord-4c3f34822216472c8935f8b7d5cf449b
Quelldatensatz
uspto-grants-1990_08
Patentnummer
US04952722

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