HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Methoxyphenyl)piperazine → 1-{3-(p-Fluoroanilino)propyl}-4-(o-methoxyphenyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (3-Chloropropyl)-(4-fluorophenyl)amine | HCID 12769738 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-{3-(p-Fluoroanilino)propyl}-4-(o-methoxyphenyl)piperazine | HCID 13314240 | — |
Reaction Steps
A mixture of 1.9 g of N-(3-chloropropyl)-p-fluoroaniline, 1.9 g of 1-(o-methoxyphenyl)piperazine, 0.5 g of sodium carbonate and 50 ml of dimethylformamide was heated at 80°-90° C for 15 hours. After cooling, the reaction mixture was poured into water and extracted with benzene. The extract was washed with water, dried over sodium sulfate and evaporated under reduced pressure to give 1-{3-(p-fluoroanilino)propyl}-4-(o-methoxyphenyl)piperazine, m.p. 79°-80° C; recrystallized from cyclohexane, m.p. 84°-84.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04017624 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-3b3007affacf4d99a309c3ff1fc5fb00 |
| Source note | uspto-grants-1977_04 |