HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014205Generated: October 30, 2026
Potassium Carbonate → 1-[3-(Methyloxy)-4-nitrophenyl]-4-propylpiperazine
https://huagongshe.com/reaction/1014205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | 1-(3-Methoxy-4-nitrophenyl)piperazine | HCID 3967409 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[3-(Methyloxy)-4-nitrophenyl]-4-propylpiperazine | HCID 59860266 | 72% |
Reaction Steps
A solution of 1-[3-(methyloxy)-4-nitrophenyl]piperazine (1.78 g, 7.51 mmol), 1-iodopropane (1.92 g, 11.3 mmol), and potassium carbonate (4.15 g, 30.0 mmol) in acetonitrile (50 mL) was heated in a pressure vessel at 80° C. for 24 hours. The reaction was cooled and the acetonitrile was removed under reduced pressure. The solids were dissolved in methylene chloride/water. The organic layer was dried over sodium sulfate and the solvent removed under reduced pressure. The resultant residue was purified by chromatography on SiO2 (10% MeOH/CH2CL2 with 0.2% NH3) to give 1-[3-(methyloxy)-4-nitrophenyl]-4-propylpiperazine as a pale yellow solid (1.5 g, 5.4 mmol, 72% yield). 1H NMR (400 MHz, CDCl3) δ ppm 0.94 (t, J=7.32 Hz, 3H), 1.51-1.61 (m, 2 H), 2.34-2.42 (m, 2 H), 2.59 (s, 4 H), 3.38-3.45 (m, 4 H), 3.95 (s, 3 H), 6.31 (d, J=2.20 Hz, 1 H), 6.42 (dd, J=9.34, 2.38 Hz, 1 H), 8.00 (d, J=9.52 Hz, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07981903B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-9b57210ebf0f45afa3d914c9e44f6e24 |
|---|
| Source note | uspto-grants-2011_07 |
|---|