Reacción #549509
ord-578e89c8bb154f0f84c922b4c7af9d3e
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1TemperaturaThe resulting mixture is then heated
- 2Temperaturaat reflux for about two hours
- 3Temperaturato cool
- 4FiltraciónThe mixture is then filtered from the catalyst
- 5Concentraciónconcentrated in vacuo
- 6Otroto remove the ethanol
- 7Lavadowashed with water
- 8Secadodried over sodium sulfate
- 9Filtraciónfiltered
- 10Concentraciónconcentrated in vacuo
Procedimiento
A solution of 1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentanone (13.2 g., 0.04 mole) in 50 cc of anhydrous ethanol is added dropwise over about 20 minutes to a stirred solution of 1,3-diamino-2-hydroxypropane (25 g., 0.27 mole) in 200 cc of ethanol. The resulting mixture is then heated at reflux for about two hours, allowed to cool, 1.0 g. platinum oxide added, and the mixture reduced under a 40 psi hydrogen atmosphere until hydrogen uptake ceases. The mixture is then filtered from the catalyst, concentrated in vacuo to remove the ethanol, the oily residue taken up in ether (250 cc.), washed with water, dried over sodium sulfate, filtered and concentrated in vacuo to yield the product 1-amino-3-[1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentylamino]-2-propanol as a pale yellow oil.