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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl itaconate | HCID 69240 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | HCID 178516071 | HCID 178516071 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 1-(4-methoxybenzyl)-5-oxopyrrolidine-3-carboxylate | HCID 4093874 | 85.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244747B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-4ffb4fad867844928bd5925445c46d94 |
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| Source note | uspto-grants-2007_07 |
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