HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539728Generated: October 29, 2026
Tert-butyl 4-(3-nitrophenethyl)piperazine-1-carboxylate → Tert-butyl 4-(3-aminophenethyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/539728
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyl 4-(3-nitrophenethyl)piperazine-1-carboxylate | HCID 57597097 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl 4-(3-aminophenethyl)piperazine-1-carboxylate | HCID 57597088 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08871769B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-307a610e647d4fb8b155bf525326eced |
|---|
| Source note | uspto-grants-2014_10 |
|---|