Reacción #72975

Ecuación de reacción

tert-butyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate

→

tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate

Disolventes

ethanol

Condiciones de reacción

Tratamiento posterior

1. 1
   FiltraciónThe mixture was filtered through CELITE
2. 2
   Filtraciónfilter agent
3. 3
   Concentraciónthe filtrate was concentrated

Procedimiento

A mixture of tert-butyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate (20.42 g, 78.4 mmol) and 20% palladium hydroxide on carbon (1.21 g) in ethanol (250 mL) was hydrogenated at 40 psi (2.8×105 Pa) for 3 d on a Parr apparatus. More 20% palladium hydroxide on carbon (1.0 g) was added and the hydrogenation was continued for 2 more days. The mixture was filtered through CELITE filter agent and the filtrate was concentrated to provide tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate, which was concentrated from toluene (200 mL) to remove residual ethanol before use in the next reaction.

Fuente