HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → n-[1-(p-Nitrophenethyl)-4-piperidinyl]-n-phenylpropionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Nitrophenethyl bromide | HCID 79266 | — |
| Reactant | 4-(N-Propionylaniline)piperidine | HCID 259381 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | n-[1-(p-Nitrophenethyl)-4-piperidinyl]-n-phenylpropionamide | HCID 13408923 | 56% |
Reaction Steps
A suspension of norfentanyl of Example 4 (6.71 g, 0.029 mol), p-nitrophenethylbromide (7.178 g, 0.0372 mol), potassium carbonate (19 g, 0.14 mol) and a few crystals of sodium iodide in 4-methyl-2-pentanone (200 ml) was stirred overnight at reflux, under nitrogen. After cooling to room temperature, the precipitate was removed by filtration and the solution concentrated under reduced pressure. The dark residue was dissolved in ethyl acetate (200 ml) and washed with water (2×100 ml), dried over sodium sulfate, filtered and the solvent removed in vacuo. The residue was purified by column chromatography (silica gel, 10% MeOH/90% CHCl3 v/v) to give the title compound as a yellow solid (5.33 g, 56% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109310B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-f5ba4c2185494aaba25de8ea0744f985 |
| Source note | uspto-grants-2006_09 |