HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 4-(cyclopropylcarbonyl)piperazine-1-carboxylate → 1-(Cyclopropylcarbonyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 4-(cyclopropylcarbonyl)piperazine-1-carboxylate | HCID 23069850 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(Cyclopropylcarbonyl)piperazine | HCID 2064235 | 97.3% |
Reaction Steps
In 100 mL of ethanol was dissolved benzyl 4-(cyclopropylcarbonyl)piperazine-1-carboxylate (3.00 g, 10.4 mmol), and 1.5 g of 10% palladium-carbon was added thereto, followed by stirring at room temperature under hydrogen atmosphere overnight. The palladium-carbon was removed by filtration, and the filtrate was evaporated to give the title compound (1.50 g, 97.3%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07619100B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-82ab1b217edd4a61af11c48f6b174f2c |
| Source note | uspto-grants-2009_11 |