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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651659Generated: October 26, 2026

Methylamine → 5-(3-Amino-4-chlorophenyl)-5-hydroxy-1-methylpyrrolidin-2-one

https://huagongshe.com/reaction/1651659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant3-(3-Amino-4-chlorobenzoyl)propionic acidHCID 14256802—
SolventTetrahydrofuranHCID 8028—
Product5-(3-Amino-4-chlorophenyl)-5-hydroxy-1-methylpyrrolidin-2-oneHCID 14256803—

Reaction Steps

42.8 g of ethyl chloroformate are metered into a solution of 60 g of 4-(3-amino-4-chlorophenyl)-4-oxobutyric acid and 27.8 g of triethylamine in 500 ml of tetrahydrofuran in such a way that the temperature does not exceed 10° C. The mixture is stirred in the icebath for a further 10 min and then, while maintaining the cooling, a solution of 35 g of gaseous methylamine in 250 ml of tetrahydrofuran is added, during which a temperature of 25° C. should not be exceeded. After stirring for a further 45 minutes in the icebath, the solvent is removed by distillation, water is added to the residue, and the crystalline precipitate is filtered off. Crystals of melting point 154° C. (from ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929643
Source datasetuspto-grants-1990_05
ORD IDord-8beb8b841f1c41acbc90ba7c0d4a88dc
Source noteuspto-grants-1990_05