HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21394Generated: October 25, 2026
Potassium Carbonate → 3-(R, S)-(1-cyano-1,1-diphenylmethyl)-1-(3,4-methylenedioxybenzyl)piperidine
https://huagongshe.com/reaction/21394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Benzodioxole, 5-(chloromethyl)- | HCID 88713 | — |
| Reactant | 3-(R,S)-(1-cyano-1,1-diphenylmethyl)piperidine | HCID 13633746 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(R, S)-(1-cyano-1,1-diphenylmethyl)-1-(3,4-methylenedioxybenzyl)piperidine | HCID 21224090 | — |
Reaction Steps
A mixture containing 3-(R,S)-(1-cyano-1,1-diphenylmethyl)piperidine (0.27 g), 3,4-methylenedioxybenzyl chloride (0.18 g), anhydrous potassium carbonate (0.3 g) and acetonitrile (10 ml) was heated under reflux for 16 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 (2×30 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a gum which was purified by column chromatography on silica eluting with dichloromethane containing methanol (0% up to 2%). The product-containing fractions were combined and concentrated in vacuo to give the title compound as a colourless solid, yield 0.2 g, m.p. 127°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05422358 |
|---|
| Source dataset | uspto-grants-1995_06 |
|---|
| ORD ID | ord-f4ebb4a7445c4ab394c698709b23831b |
|---|
| Source note | uspto-grants-1995_06 |
|---|