Réaction #67431
ord-7d217eca82a542c5b4d2f1a5e11e01ee
Équation de réaction
Réactifs
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1FiltrationThe catalyst was filtered off
- 2Concentrationthe filtrate was concentrated to dryness
Mode opératoire
A suspension of (4′-cyano-biphenyl-3-yl)-carbamic acid tert-butyl ester (7.6 g, 26 mmol) and Raney Ni (1 g) in EtOH (500 mL) and NH3.H2O (10 mL) was hydrogenated under 50 psi of H2 at 50° C. for 6 h. The catalyst was filtered off and the filtrate was concentrated to dryness to give (4′-aminomethyl-biphenyl-3-yl)-carbamic acid tert-butyl ester, which was used directly in next step.