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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862202Generated: October 29, 2026

Methyl iodide → 1-tert-Butyl 4-ethyl 4-methylpiperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/862202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
Reactant1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylateHCID 2758812—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-tert-Butyl 4-ethyl 4-methylpiperidine-1,4-dicarboxylateHCID 16218276105%

Reaction Steps

To a stirring solution of diisopropylamine (20.0 mmol, 2.02 g) in THF (50 mL) cooled to -78° C. was added n-butyllithium (21.7 mmol, 8.68 mL of a 2.5M solution in hexanes). N-tert-butoxycarbonyl isonipecotic acid ethyl ester (16.7 mmol, 4.5 g) was then added dropwise followed by methyl iodide (16.7 mmol, 2.37 g)and the reaction allowed to warm to room temperature. The mixture was then diluted with ethyl acetate (500 mL) and washed with water (1×200 mL), 10% KHSO4 (200 mL) and brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure to give 4.76 g of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05717100
Source datasetuspto-grants-1998_02
ORD IDord-ab6774ca427942348b8db0d3699ec6fe
Source noteuspto-grants-1998_02