Reaktion #54455

Reaktionsgleichung

2,2,6-trimethylcyclohexanone

3-hydroxy-3,7-dimethyl-nona-4,6,8-trien-1-yne

ammonium chloride

ethyl bromide

magnesium

→

7-hydroxy-3,7-dimethyl-9-(1-hydroxy-2,2,6-trimethylcyclohexyl)-nona-1,3,5-trien-8-yne

Lösungsmittel

benzene

benzene

diethyl ether

ether

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturthe mixture was heated
2. 2
   Temperaturto reflux for 30 minutes
3. 3
   Temperaturthe mixture refluxed 30 minutes
4. 4
   Temperaturthe mixture refluxed for 15 minutes
5. 5
   WaschenThe organic phase was washed with brine
6. 6
   Sonstigedried
7. 7
   Einengenconcentrated

Vorschrift

A solution of ethyl bromide (1.75 g.) in diethyl ether was added to a suspension of magnesium (0.385 g.) in ether and the mixture was heated to reflux for 30 minutes. A solution of the alcohol, 3-hydroxy-3,7-dimethyl-nona-4,6,8-trien-1-yne, (1.0 g.) in dry benzene was added and the mixture refluxed 30 minutes. A solution of 2,2,6-trimethylcyclohexanone (1.12 g.) in benzene was added and the mixture refluxed for 15 minutes and poured into saturated aqueous ammonium chloride solution. The organic phase was washed with brine dried and concentrated to give 7-hydroxy-3,7-dimethyl-9-(1-hydroxy-2,2,6-trimethylcyclohexyl)-nona-1,3,5-trien-8-yne which was chromatographed on activity III alumina to give pure 7-hydroxy-3,7-dimethyl-9-(1-hydroxy-2,2,6-trimethyl-cyclohexyl)-nona-1,3,5-trien-8-yne.

Quelle