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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412295Generated: October 30, 2026

Ammonium formate → {2-[3-((R)-2-Aminopropyl)phenyl]ethyl}carbamic Acid tert-Butyl Ester

https://huagongshe.com/reaction/2412295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant(2-{3-[(R)-2-((R)-1-phenylethylamino)propyl]phenyl}ethyl)carbamic acid tert-butyl esterHCID 66781838—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product{2-[3-((R)-2-Aminopropyl)phenyl]ethyl}carbamic Acid tert-Butyl EsterHCID 66782120—

Reaction Conditions

Temperature50 °C

Reaction Steps

A stirred solution of (2-{3-[(R)-2-((R)-1-phenylethylamino)propyl]phenyl}ethyl)-carbamic acid tert-butyl ester (1.54 g, 4.02 mmol), palladium hydroxide on carbon (10 wt. %, ˜50% water, 2.24 g, 0.805 mmol), and ammonium formate (1.27 g, 20.1 mmol) in EtOH (50.0 mL) was heated gradually to 50° C. and then stirred at 50° C. for 1.5 h. The reaction mixture was filtered through a pad of Celite and the filtrate was concentrated under reduced pressure to give the title compound, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816088B2
Source datasetuspto-grants-2014_08
ORD IDord-88dba7251d9046f985d5851d647b43fa
Source noteuspto-grants-2014_08