HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1-Benzyl-4-methyl-4-phenylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 1-Benzyl-4-methylpiperidin-4-ol | HCID 10845913 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-Benzyl-4-methyl-4-phenylpiperidine | HCID 10801662 | 104% |
Reaction Steps
1-Benzyl-4-methylpiperidin-4-ol (4.81 g, 23.4 mmol, 1.00 equiv) was added to a suspension of AlCl3 (15.62 g, 117 mmol, 5.00 equiv) in benzene (100 mL) at room temperature under argon. The mixture was stirred at reflux for 24 hours, then cooled and poured cautiously into ice water (100 g of ice plus 50 mL of water). The aqueous phase was adjusted to pH 11-12 by addition of 6N aqueous NaOH at 0° C., and extracted with EtOAc (3×100 mL). The combined organic solutions were dried over MgSO4 and concentrated. The residue was purified by flash chromatography (SiO2, hexane-Et2O 19:1 to 9:1 followed by hexane-EtOAc 3:1) to give 3.23 g (52%) of brown oil, which was characterized spectroscopically.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211198B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-e63088929bf3495e8c42a7d4de85e22a |
| Source note | uspto-grants-2001_04 |