Reaktion #531528

Reaktionsgleichung

potassium carbonate

3-[4-(1,1-dimethylheptyl)-2-hydroxyphenyl]-4-(3-phenylpropyl)-4-piperidinol

p-toluenesulfonic acid monohydrate

toluene

→

title compound

3-[4-(1,1-Dimethylheptyl)-2-hydroxyphenyl]-4-(3-phenylpropyl)-1,2,5,6-tetrahydropyridine

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONA mixture of 2.0 g
2. 2
   Temperaturunder reflux for 2 hours with a Dean Stark trap
3. 3
   TemperaturThe reaction mixture is cooled
4. 4
   workup.ADDITIONadded to 100 ml
5. 5
   ExtraktionThe dichloromethane extract along with two additional 200 ml
6. 6
   Trocknendichloromethane extracts of the basic phase is dried over magnesium sulfate
7. 7
   Sonstigeevaporated
8. 8
   SonstigeThe residue is crystallized from ether-pentane

Vorschrift

A mixture of 2.0 g. (4.57 mmols.) of 3-[4-(1,1-dimethylheptyl)-2-hydroxyphenyl]-4-(3-phenylpropyl)-4-piperidinol, 0.95 g. (5.0 mmols.) of p-toluenesulfonic acid monohydrate and 100 ml. of toluene is heated under reflux for 2 hours with a Dean Stark trap. The reaction mixture is cooled and added to 100 ml. of 20% potassium carbonate-200 ml. dichloromethane. The dichloromethane extract along with two additional 200 ml. dichloromethane extracts of the basic phase is dried over magnesium sulfate and evaporated. The residue is crystallized from ether-pentane to yield the title compound.

Quelle