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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Piperidin-4-ylmethyl-piperidine-1-carboxylic acid t-butyl ester | HCID 49761197 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,1-Dimethylethyl 4-{[1-(1-methylethyl)-4-piperidinyl]methyl}-1-piperidinecarboxylate | HCID 68888845 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07638631B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-64d3a6b4d34046f9998aafb24779ff0f |
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| Source note | uspto-grants-2009_12 |
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