HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Benzoate → 1-Benzoylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Benzoate | HCID 7150 | — |
| Reactant | Diethylaluminum chloride | HCID 7277 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Methylpiperazine | HCID 66057 | — |
| Reactant | Chlorodimethylaluminum | HCID 79147 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Benzoylpiperazine | HCID 762654 | 105,129.398% |
Reaction Steps
To a stirred solution of 2-methylpiperazine (10.0 g, 0.1 mol) in dry CH2Cl2 (500 ml) under argon was added a solution of 1.0 M Me2AlCl or Et2AlCl in hexanes (100 ml, 0.1 mmol) and methyl benzoate (12.4 ml, 0.1 mmol) at room temperature. The reaction mixture was then stirred for 2 days before 2N NaOH (200 ml) was added. Aqueous layer was extracted with EtOAc (3×100 ml). The combined organic layer was dried over MgSO4 and concentration of solution provided 20.0 g of crude product (98%), with was pure enough for the further reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06469006B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-08635df05a534bdeb0dfde8159a0fd53 |
| Source note | uspto-grants-2002_10 |