Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639728Generated: October 30, 2026

Tert-butyl 4-(3-nitrophenethyl)piperazine-1-carboxylate → Tert-butyl 4-(3-aminophenethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1639728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(3-nitrophenethyl)piperazine-1-carboxylateHCID 57597097—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductTert-butyl 4-(3-aminophenethyl)piperazine-1-carboxylateHCID 5759708863%

Reaction Steps

A Parr glass liner was charged with tert-butyl 4-(3-nitrophenethyl)piper-azine-1-carboxylate (7C, 1.0 eq) and methanol (about 0.2 M 7C in MeOH). To this solution was added a slurry of 12.5 wt eq of 10% Pd/C in methanol. The reaction mixture was sealed in a Parr hydrogenation vessel and subjected to 3 pressurization/venting cycles with H2. The reaction mixture was allowed to proceed at room temperature and 45 psi H2 for 2.5 h. The reaction mixture was then charged with 12.5 wt eq of Pd(OH)2/C and the vessel was repressurized with hydrogen (45 psi). After 1 hr, the reaction mixture was filtered through a pad of diatomaceous earth, the diatomaceous earth washed with MeOH, and the combine organic layers concentrated in vacuo to provide the desired tert-butyl 4-(3-aminophenethyl)piperazine-1-carboxylate (7D, 63%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110595B2
Source datasetuspto-grants-2012_02
ORD IDord-cf14aed9c7dd496084a884d7e34281fe
Source noteuspto-grants-2012_02