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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869621Generated: October 30, 2026

Isopropyl iodide → 1,1-Dimethylethyl 4-{[1-(1-methylethyl)-4-piperidinyl]methyl}-1-piperidinecarboxylate

https://huagongshe.com/reaction/1869621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Piperidin-4-ylmethyl-piperidine-1-carboxylic acid t-butyl esterHCID 49761197—
SolventAcetonitrileHCID 6342—
Product1,1-Dimethylethyl 4-{[1-(1-methylethyl)-4-piperidinyl]methyl}-1-piperidinecarboxylateHCID 68888845—

Reaction Conditions

Temperature50 °C

Reaction Steps

1,1-Dimethylethyl 4-(4-piperidinylmethyl)-1-piperidinecarboxylate (may be prepared as described in Description 2) (3 g), isopropyl iodide (3.2 ml) and K2CO3 (2.94 g) were combined in acetonitrile (70 ml) and the reaction mixture heated at 50° C. overnight. The reaction was allowed to cool to room temperature, filtered and evaporated. The residue was dissolved in diethylether (50 ml) and washed successively with water (50 ml), saturated sodium thiosulphate solution (50 ml), saturated brine (50 ml) and dried (Na2SO4). The solvent was evaporated to give the title compound (D3) as a pale yellow oil (3.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638631B2
Source datasetuspto-grants-2009_12
ORD IDord-64d3a6b4d34046f9998aafb24779ff0f
Source noteuspto-grants-2009_12