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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931306Generated: November 1, 2026

Methyl iodide → 1-tert-Butyl 3-ethyl 3-methylpiperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/1931306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-Tert-butyl 3-ethylpiperidine-1,3-dicarboxylateHCID 75692153—
SolventTetrahydrofuranHCID 8028—
Product1-tert-Butyl 3-ethyl 3-methylpiperidine-1,3-dicarboxylateHCID 20585394—

Reaction Steps

A THF (5 mL) solution of 1-tert-butyl 3-ethylpiperidine-1,3-dicarboxylate (1 g, 3.89 mmol) was added dropwise to a THF (15 mL) solution of lithium diisopropylamide (5.83 mmol) in a nitrogen atmosphere at −78 degrees over 5 minutes. The mixture was raised to room temperature, and stirred for 50 minutes. The temperature of the reaction mixture was lowered to −78 degrees again, and methyl iodide (1.21 mL, 19.43 mmol) was added dropwise at −78 degrees over 5 minutes. The reaction mixture was then raised to room temperature, and stirred for 5 hours. After being added to a saturated ammonium chloride aqueous solution, the reaction mixture was stirred for a while, and extracted with diethyl ether. The organic layer was collected, washed once with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was then purified using silica gel column chromatography to obtain the target (698 mg, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188280B2
Source datasetuspto-grants-2012_05
ORD IDord-530f989bae0b44329767897ee4449098
Source noteuspto-grants-2012_05