HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584164Generated: October 26, 2026
Potassium Carbonate → 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)-1-(4-hydroxymethylphenethyl)piperidine
https://huagongshe.com/reaction/1584164
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | [4-(2-Bromoethyl)phenyl]methanol | HCID 22337010 | — |
| Reactant | 3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidine | HCID 22853758 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)-1-(4-hydroxymethylphenethyl)piperidine | HCID 22853754 | — |
Reaction Steps
A mixture containing 3(R)-(+)-(1-cyano-1,1,-diphenylmethyl)-piperidine (0.28 g), 4- hydroxymethylphenethyl bromide (0.22 g), anhydrous potassium carbonate (0.28 g) and acetonitrile (10 ml) was heated under reflux for 5 hours. The mixture was partitioned between dichloromethane (30 ml) and 10% aqueous potassium carbonate (20 ml), the layers separated, and the aqueous layer extracted with dichloromethane (2×20 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 0.21 g, m.p. 110-114° C., [α]D25 -16.2° (c, 1.0, CH2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05932594 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-8849366b759b4372abbd2b0602781019 |
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| Source note | uspto-grants-1999_08 |
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