Reaktion #572125

Reaktionsgleichung

hydrogen

2,2,6,6-tetramethyl-4-piperidone

ammonium chloride

potassium carbonate

→

title compound

Bis(2,2,6,6-tetramethyl-4-piperidyl)amine

Lösungsmittel

methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeat room temperature
2. 2
   Sonstigefor 8 hours
3. 3
   FiltrationThe platinum catalyst was filtered off
4. 4
   Extraktionthe filtrate was extracted with benzene
5. 5
   TrocknenThe extract was dried over anhydrous potassium carbonate
6. 6
   workup.DISTILLATIONthe benzene was distilled off
7. 7
   workup.DISTILLATIONThe resulting oil was distilled under a high vacuum

Vorschrift

1.0 g of platinum oxide was added to a suspension of 50.0 g of 2,2,6,6-tetramethyl-4-piperidone and 109 g of ammonium chloride in 200 ml of methanol. The resulting mixture was then hydrogenated in a hydrogen atmosphere, employing a Parr hydrogenation apparatus at room temperature for 8 hours. At the end of this time, the reaction mixture was poured into an aqueous solution of potassium carbonate. The platinum catalyst was filtered off and the filtrate was extracted with benzene. The extract was dried over anhydrous potassium carbonate and then the benzene was distilled off. The resulting oil was distilled under a high vacuum, to give the title compound in the form of an oil boiling at 135°-139° C./2 mmHg (267 Pascals). This product was purified by column chromatography through silica gel, eluted with a 5:5:1 by volume mixture of ethyl acetate, ethanol and triethylamine, to give the title compound in the form of crystals melting at 77°-78° C.

Quelle