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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569215Generated: October 31, 2026

Methyl iodide → (+/-) 5,5-Diethoxycarbonyl-1-methyl-4-phenyl-pyrrolidin-2-one

https://huagongshe.com/reaction/569215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-Phenyl-5,5-dicarbethoxy-2-pyrrolidinoneHCID 98627—
SolventDimethylformamideHCID 6228—
Product(+/-) 5,5-Diethoxycarbonyl-1-methyl-4-phenyl-pyrrolidin-2-oneHCID 1382597699.6%

Reaction Steps

A solution of 100 g (0.33 mole) of (±) 5,5-diethoxycarbonyl-4-phenylpyrrolidin-2-one in 500 ml of absolute dimethylformamide was added dropwise to a suspension of 9.64 g (0.36 mole) of sodium hydride in 200 ml of absolute dimethylformamide at room temperature under an N2 atmosphere. The mixture was subsequently stirred at room temperature until the evolution of gas had ended, a solution of 93.7 g (0.66 mole) of methyl iodide in 50 ml of absolute dimethylformamide was then added and the mixture was stirred at room temperature until all the starting material had reacted (about 1 hour, thin layer chromatography check). The reaction mixture was poured into 2 l of buffer solution, pH=7, and extracted five times with 600 ml of diethyl ether each time. Drying of the organic extracts (MgSO4) and stripping off of the solvent in vacuo gave 105 g (99.6%) of the title compound (95% pure according to (the 1H-NMR spectrum), which was further reacted directly. A sample was distilled in a bulb tube (boiling point0.5 : 240° C.) for analysis, Rf : 0.36 (toluene/ethyl acetate: 2/1),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731456
Source datasetuspto-grants-1988_03
ORD IDord-fbaf67ebf4a249c48a9427d2339d61ef
Source noteuspto-grants-1988_03