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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640606Generated: October 29, 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/640606

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 numberUS07691902B2
Source datasetuspto-grants-2010_04
ORD IDord-321c9188d6214170aef38b9466bb1e56
Source noteuspto-grants-2010_04