HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21390Generated: October 25, 2026
Potassium Carbonate → 3-(R)-(1-cyano-1,1-diphenylmethyl)-1--(3,4-dichlorophenethyl)piperidine
https://huagongshe.com/reaction/21390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Bromoethyl)-1,2-dichlorobenzene | HCID 15149389 | — |
| Reactant | 3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidine | HCID 22853758 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(R)-(1-cyano-1,1-diphenylmethyl)-1--(3,4-dichlorophenethyl)piperidine | HCID 21311312 | — |
Reaction Steps
A mixture containing 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)piperidine (0.28 g), 3,4-dichlorophenethyl bromide (0.255 g), anhydrous potassium carbonate (0.3 g) and acetonitrile (10 ml) was heated under reflux for 8 hours. The mixture was partitioned between dichlorometbane (30 ml) and 10% aqueous potassium carbonate (20 ml), the layers separated and the aqueous layer extracted with dichloromethane (3×70 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated inn vacuo to give an oil which was purified by column chromatograpby on silica eluting with dichloromethane containing hexane (30%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from acetonitrile to give the title compound, yield 0.233 g, m.p. 139°-142° C.
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-2b313ee99fad42879db9e4efd08876bc |
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| Source note | uspto-grants-1995_06 |
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