HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21386Generated: October 25, 2026
Phenethyl bromide → 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)-1-phenethylpiperidine
https://huagongshe.com/reaction/21386
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidine | HCID 22853758 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)-1-phenethylpiperidine | HCID 22853756 | — |
Reaction Steps
A mixture containing 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)piperidine (1 g), phenethyl bromide (0.-67 g), anhydrous potassium carbonate (1.5 g) and acetonitrile (25 ml) was heated under reflux for 4 hours. The mixture was partitioned between dichloromethane (50 ml) and 10% aqueous potassium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (3×30 ml)--. The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give an oil which was purified by column chromatography on silica eluting with hexane containing dichloromethane (30% up to 70%) then dichloromethane containing methanol (0% up to 5%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from acetonitrile to give the title compound as colourless rhombs, yield 0.72 g, m.p. 134°-138° C., [α]D25 +13.3° (C 1.0, CH2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05422358 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-19fb6cb68a014b86af7f9d7ebbf543ed |
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| Source note | uspto-grants-1995_06 |
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