HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 4-(4-Nitrophenyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Phenylpiperidine | HCID 69873 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(4-Nitrophenyl)piperidine | HCID 15925817 | — |
Reaction Steps
A solution of conc. H2SO4 (2.65 mL) in AcOH (40 mL) and a solution of conc. HNO3 (2.1 mL) in AcOH (20 mL) are added sequentially and dropwise to a solution of 4-phenylpiperidine in AcOH (40 mL), maintaining the temperature below 20° C. Then, conc. H2SO4 (40 mL) is added (no cooling applied; internal temperature reaches 60° C.). The reaction mixture is allowed to cool to RT, poured onto ice/water (100 g), neutralized by addition of solid NaHCO3 (150 g), and extracted with DCM. The organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. The residue is purified by trituration in Et2O to afford the title compound as a yellow solid. ESI-MS: 207.1 [MH]+; tR=2.42 min (system 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759517B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-5f6a682a90d44a2ab2ace0188ad48486 |
| Source note | uspto-grants-2014_06 |