HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → HCID 13537610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | HCID 20252669 | HCID 20252669 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Acetone diethylether | HCID 21584533 | — |
| Product | HCID 13537610 | HCID 13537610 | 102.9% |
Reaction Steps
A solution of 3.5 g of (5-bromomethylisoxazol-3-yl)-phenylmethanone in 100 ml of Et2O was added dropwise to a solution of 8.6 g of phenylpiperazine in 375 ml of 20% acetone/Et2O. The resulting mixture was stirred at room temperature for 72 hours. This mixture was washed with water and brine, and dried over MgSO4. Concentration of the product gave an oil, which was taken up in 500 ml of CH2Cl2 and stirred with 20 g of silica gel overnight. The silica was removed by filtration and washed with 500 ml of CH2Cl2. The combined filtrates were concentrated to give 4.7 g of an oil which solidified on standing. Recrystallization from ethanol yielded 3.1 g (69%) of platelets, m.p. 100°-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04562187 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-9a33bd7f6971474695ec3cc355b17aea |
| Source note | uspto-grants-1985_12 |