HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-Benzyl-4-cyano-4-phenylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Phenylpiperidine-4-carbonitrile hydrochloride | HCID 3084973 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 1-Benzyl-4-cyano-4-phenylpiperidine | HCID 191408 | — |
Reaction Steps
4-Phenyl-4-cyano-piperidine hydrochloride (10 g, 44.9 mmol), Benzyl bromide (5.4 mL, 45.4 mmol), and potassium carbonate (25.2 g, 182.3 mmol) were combined in THF/water (80 mL/20 mL). After 18 hours the reaction mixture was partitioned between water and dichloromethane. The organic layer was separated and extracted with water, dried over MgSO4, filtered and evaporated in vacuo to give a residue. The residue was recrystallized from hexane to give 4-phenyl -4-cyano-1-benzyl-piperidine as a solid: mp=73°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05861416 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-7196131bc85b48c180eb5cb7a5f2c8d7 |
| Source note | uspto-grants-1999_01 |