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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Benzodioxole, 5-(chloromethyl)-HCID 88713—
Reactant3-(R,S)-(1-cyano-1,1-diphenylmethyl)piperidineHCID 13633746—
SolventAcetonitrileHCID 6342—
Product3-(R, S)-(1-cyano-1,1-diphenylmethyl)-1-(3,4-methylenedioxybenzyl)piperidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05422358
Source datasetuspto-grants-1995_06
ORD IDord-f4ebb4a7445c4ab394c698709b23831b
Source noteuspto-grants-1995_06