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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510365Generated: November 3, 2026

Methyl iodide → 1-Benzyl 3-ethyl 3-methyl-4-oxopyrrolidine-1,3-dicarboxylate

https://huagongshe.com/reaction/1510365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Benzyl 3-ethyl 4-oxopyrrolidine-1,3-dicarboxylateHCID 15043278—
SolventAcetoneHCID 180—
Product1-Benzyl 3-ethyl 3-methyl-4-oxopyrrolidine-1,3-dicarboxylateHCID 5728013796.3%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of ethyl 1-benzyloxycarbonyl-4-oxopyrrolidine-3-carboxylate (1.0 g, 3.4 mmol) in acetone (30 mL), potassium carbonate (0.95 g, 6.9 mmol) and methyl iodide (1 mL) were added, and the mixture was stirred at 45° C. for 1 hour. The reaction mixture was concentrated under reduced pressure, and water (20 mL) was added to the concentrate. The mixture was extracted with ethyl acetate (20 mL×3). The extract was washed with 10% aqueous solution of sodium thiosulfate (20 mL) and saturated aqueous solution of sodium chloride (20 mL) in this order, and dried with anhydrous sodium sulfate. After the filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate, 4:1) to obtain 1.0 g (95%) of the title compound as a pale yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211910B2
Source datasetuspto-grants-2012_07
ORD IDord-efc37c65c025447d9a1c795779cc7a47
Source noteuspto-grants-2012_07