HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990097Generated: October 30, 2026
Methyl iodide → 1-tert-Butyl 3-ethyl 3-methylpiperidine-1,3-dicarboxylate
https://huagongshe.com/reaction/990097
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1-Tert-butyl 3-ethyl piperidine-1,3-dicarboxylate | HCID 357727 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-tert-Butyl 3-ethyl 3-methylpiperidine-1,3-dicarboxylate | HCID 20585394 | 90% |
Reaction Steps
Potassium bis(trimethylsilyl)amide (1200 ml, 0.5M in toluene, 0.6 mol) was added to a 3-necked 3-l flask equipped with an overhead stirrer, followed by tetrahydrofuran (90 ml) and the solution was cooled to −78° C. Ethyl N-(t-butyloxycarbonyl)nipecotate (100 g, 0.39 mol) in tetrahydrofuran (90 ml) was added dropwise and the resulting solution allowed to age for 15 minutes. Iodomethane (37.4 ml, 85.2 g, 0.6 mol) was added dropwise to the stirred solution keeping the temperature below −70° C. The resulting mixture was stirred at room temperature overnight and was evaporated under reduced pressure. The residue was partitioned between ethyl acetate and water and the organic layer was washed with brine, dried (sodium sulphate) and evaporated to give a yellow oil. This was purified on a plug of silica using dichloromethane as eluant to afford the product (94 g, 90%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458830B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-fd029e7ae3814af1b8eb4f75ee4b2fb5 |
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| Source note | uspto-grants-2002_10 |
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