HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 2,4-diphenylpiperazine-1-carboxylate → 1,3-Diphenylpiperizine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 2,4-diphenylpiperazine-1-carboxylate | HCID 67506058 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 1,3-Diphenylpiperizine | HCID 54176605 | 93.2% |
Reaction Steps
A solution of benzyl 2,4-diphenylpiperazine-1-carboxylate (0.17 g, 0.45 mmol) and 5% Pd on carbon (0.1 g) in tetrahydrofuran/methanol 5:1 (10 mL) was stirred under hydrogen (1 atm) for 4.5 hours. The reaction was filtered through celite and concentrated to give the title compound 1,3-diphenylpiperizine (0.10 g, 93% yield) as an oil. MS (EI) for C16H18N2: 239 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637499B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-c3b99b9973024e79808dd94f102614a0 |
| Source note | uspto-grants-2014_01 |