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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796942Generated: November 3, 2026

(S)-(+)-N-(2,3-Epoxypropyl)phthalimide → (S)-4-(4-(5-(aminomethyl)-2-oxooxazolidin-3-yl)phenyl)morpholin-3-one

https://huagongshe.com/reaction/1796942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(+)-N-(2,3-Epoxypropyl)phthalimideHCID 719412—
Reactant4-(4-Aminophenyl)morpholin-3-oneHCID 11194854—
ReactantWater ethanolHCID 19096565—
Product(S)-4-(4-(5-(aminomethyl)-2-oxooxazolidin-3-yl)phenyl)morpholin-3-oneHCID 11346837—

Reaction Steps

A suspension of 2-[(2S)-2-oxiranylmethyl]-1H-isoindole-1,3(2H)-dione (A. Gutcait et al. Tetrahedron Asym. 1996, 7, 1641) (5.68 g, 27.9 mmol) and 4-(4-aminophenyl)-3-morpholinone (5.37 g, 27.9 mmol) in ethanol/water (9:1, 140 ml) is heated under reflux for 14 hours (the precipitate dissolves; after some time, another precipitate is formed). The precipitate (desired product) is filtered off, washed three times with diethyl ether and dried. The combined mother liquors are concentrated under reduced pressure and, after addition of a second portion of 2-[(2S)-2-oxiranylmethyl]-1H-isoindole-1,3-(2H)-dione (2.84 g, 14.0 mmol), suspended in ethanol/water (9:1, 70 ml) and heated under reflux for 13 hours (the precipitate dissolves; after some time, another precipitate is formed). The precipitate (desired product) is filtered off, washed three times with diethyl ether and dried. Total yield: 10.14 g, 92% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034017B2
Source datasetuspto-grants-2006_04
ORD IDord-c634bc47928c40cdac410278626ce62b
Source noteuspto-grants-2006_04