HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)-1-(4chlorophenethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2-Bromoethyl)-4-chlorobenzene | HCID 23029 | — |
| Reactant | 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)piperidine | HCID 13633748 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)-1-(4chlorophenethyl)piperidine | HCID 11858413 | — |
Reaction Steps
A mixture containing 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)piperidine (0.3 g), 4-chlorophenethyl bromide (0.24 g), anhydrous potassium carbonate (0.3 g) and acetonitrile (15 ml) was heated under reflux for 7 hours. The mixture was partitioned between dichloromethane (30 ml) and 10% aqueous sodium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (2×50 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a solid which was recrystallised from aqueous methanol to give the title compound, yield 0.24 g, m.p. 188°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05422358 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-fcff833a6c514b5f99aa15dd10c0a1f5 |
| Source note | uspto-grants-1995_06 |