Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-Tert-butyl 3-ethyl piperidine-1,3-dicarboxylateHCID 357727—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTetrahydrofuranHCID 8028—
Product1-tert-Butyl 3-ethyl 3-methylpiperidine-1,3-dicarboxylateHCID 2058539490%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458830B1
Source datasetuspto-grants-2002_10
ORD IDord-fd029e7ae3814af1b8eb4f75ee4b2fb5
Source noteuspto-grants-2002_10