Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39153Generated: October 25, 2026

(4'-Cyano-biphenyl-3-yl)-carbamic acid tert-butyl ester → (4'-Aminomethyl-biphenyl-3-yl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/39153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4'-Cyano-biphenyl-3-yl)-carbamic acid tert-butyl esterHCID 67120680—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventAzane;hydrateHCID 12896473—
Product(4'-Aminomethyl-biphenyl-3-yl)-carbamic acid tert-butyl esterHCID 59206790—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524767B2
Source datasetuspto-grants-2013_09
ORD IDord-7d217eca82a542c5b4d2f1a5e11e01ee
Source noteuspto-grants-2013_09