Réaction #54279
ord-551580bfd33349668c8de1563891ed34
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1workup.ADDITIONTo the resulting solution are added 0.5 g
- 2AutreAfter the absorption of hydrogen
- 3Températurethe mixture is cooled
- 4FiltrationThen the catalyst is filtered off
- 5Concentrationthe filtrate is concentrated to dryness
- 6AutreUpon recrystallization of the crude crystalline residue from isopropyl alcohol, 12.5 g
Mode opératoire
18 g. of 1-(3,4-methylenedioxyphenyl)-2-aminoethanol hydrochloride are dissolved in 300 ml. of ethanol and 50 ml. of 80% aqueous solution of acetaldehyde. To the resulting solution are added 0.5 g. of extended Raney nickel and the mixture is heated at 70° C. in an atmosphere of hydrogen in a 1 liter-autoclave. After the absorption of hydrogen is complete, the mixture is cooled. Then the catalyst is filtered off and the filtrate is concentrated to dryness. Upon recrystallization of the crude crystalline residue from isopropyl alcohol, 12.5 g. of 1-(3,4-methylenedioxyphenyl)-2-ethylaminoethanol hydrochloride are obtained as white needles.