HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → HCID 13537621, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | HCID 20252673 | HCID 20252673 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetone diethylether | HCID 21584533 | — |
| Product | HCID 13537621 | HCID 13537621 | 115.6% |
Reaction Steps
A solution of 3.7 g of (5-bromomethylisoxazol-3-yl)-4-fluorophenylmethanone in 100 ml of Et2O was added dropwise to a solution of 5.2 g of N-phenylpiperazine in 400 ml of 20% acetone/Et2O. The resulting mixture was stirred at room temperature for 24 hours. This mixture was filtered and the solution was washed with water (2×200 ml) and saturated NaCl, and dried over MgSO4. Concentration of the product gave 5.5 g of a solid which was dissolved in 100 ml of CH2Cl2 and stirred with 5 g of SiO2. This mixture was filtered, the silica washed with CH2Cl2, and the organics were evaporated to give 3.7 g of a solid. The amine was recrystallized from 135 ml of 8% toluene/hexane to yield 2.5 g (53%) of needles, m.p. 94°-95°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04562187 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-4f29ed0a5a6c4a028d9a13ff81ea2ff3 |
| Source note | uspto-grants-1985_12 |