HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Boc-4-(4-Nitrophenyl)piperazine | HCID 3380696 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate | HCID 11011301 | — |
Reaction Steps
A mixture of 4-(4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (11) (18.9 mmol), 10% palladium-on-carbon (600 mg), ethanol (100 mL), and ethyl acetate (100 mL) is hydrogenated at room temperature and 40 psi for 2 hrs. The mixture is filtered through celite, washing with ethyl acetate (2×100 mL), and concentrated in vacuo to give 4-(4-amino-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (12) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405295B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-0e6449432c9f48c2880418c23795164b |
| Source note | uspto-grants-2008_07 |