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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923783Generated: November 2, 2026

Methyl iodide → 1-Benzyl 3-methyl 3-methylpyrrolidine-1,3-dicarboxylate

https://huagongshe.com/reaction/1923783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-Benzyl 3-methylpyrrolidine-1,3-dicarboxylateHCID 60205233—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl 3-methyl 3-methylpyrrolidine-1,3-dicarboxylateHCID 6020523575%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Lithium bis(trimethylsilyl)amide (16.4 mL, 16.4 mmol) was added to 1-benzyl 3-methylpyrrolidine-1,3-dicarboxylate (3.45 g, 13.1 mmol) in THF (20 mL) at −78° C., and the reaction was stirred at −78° C. for 20 minutes. MeI (1.10 mL, 17.7 mmol) was added, and the reaction was warmed to room temperature. After 2 hours at room temperature, the mixture was poured onto saturated ammonium chloride (20 mL), extracted with ether, washed with brine and dried over sodium sulfate. After removal of the solvent, the residue was purified by chromatography (hexane:ethyl acetate, 4:1) to give 1-benzyl 3-methyl 3-methylpyrrolidine-1,3-dicarboxylate (2.72 g, 75% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178131B2
Source datasetuspto-grants-2012_05
ORD IDord-a53ab74516544bb4850899194df807de
Source noteuspto-grants-2012_05