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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295794Generated: October 31, 2026

Dimethyl itaconate → Methyl 1-(4-methoxybenzyl)-5-oxopyrrolidine-3-carboxylate

https://huagongshe.com/reaction/1295794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl itaconateHCID 69240—
Reactant4-MethoxybenzylamineHCID 75452—
ReactantHCID 178516071HCID 178516071—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductMethyl 1-(4-methoxybenzyl)-5-oxopyrrolidine-3-carboxylateHCID 409387485.9%

Reaction Conditions

Temperature20 °C

Reaction Steps

In a 250 ml three necked flask fitted with a magnetic stirrer and reflux condenser, under inert atmosphere, 10 g (73 mmol, 1 eq) of 4-methoxy-benzylamine and 12.7 g (81 mmol, 1.1 eq) of dimethyl itaconate are dissolved in 100 ml of MeOH. The mixture is brought to reflux for 10 h, and cooled down slowly to 20° C. over 4 h and concentrated to dryness. In a 250 ml three necked flask fitted with a magnetic stirrer and Rashig column and distillation arm, under inert atmosphere, the crude intermediate and 0.69 g (7.30 mmol, 0.1 eq) of 2-hydroxypyridine are dissolved in 200 ml of toluene. The mixture is brought to reflux and the methanol formed distilled off for 8 h, until no more methanol is collected. Temperature in the pot reached 112° C. The mixture is cooled down and concentrated to dryness to give the crude ester. It is purified by column chromatography on silicagel (AcOEt/n-Hexane: 1/1 (v/v)) to afford the pure ester a1 (16.48 g, 85.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244747B2
Source datasetuspto-grants-2007_07
ORD IDord-4ffb4fad867844928bd5925445c46d94
Source noteuspto-grants-2007_07