HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenethylpiperazine → HCID 15230865, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenethylpiperazine | HCID 79214 | — |
| Reactant | HCID 19088025 | HCID 19088025 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15230865 | HCID 15230865 | 92.2% |
Reaction Steps
A solution of p-nitrophenyl 7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenyl-heptanoate (0.50 g, 1.05 mmoles) and 4-(2-phenylethyl)piperazine (0.20 g, 1.05 mmoles) in dichloromethane was allowed to stand at room temperature under stirring for 18 hours. After the solvent was evaporated in a reduced pressure, the residue was dissolved in ethylacetate and the solution was washed with aqueous potassium carbonate and water, and dried over magnesium sulfate. The solvent was evaporated and the residue was chromatographed on silica gel column with ethylacetate followed by chloroform-methanol (10:1) as eluant to give 4-[7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoyl]-(2-phenylethyl)piperazine (0.51 g, 92%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05304658 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-2f6464b38ccb49278881e02444fb9f5b |
| Source note | uspto-grants-1994_04 |