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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972186Generated: October 30, 2026

4-(4-Chlorophenoxy)aniline → 1-[4-(4-Chloro-phenoxy)-phenyl]-pyrrolidine-2,5-dione

https://huagongshe.com/reaction/1972186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorophenoxy)anilineHCID 7578—
ReactantSuccinic anhydrideHCID 7922—
ReactantThionyl ChlorideHCID 24386—
SolventTolueneHCID 1140—
Product1-[4-(4-Chloro-phenoxy)-phenyl]-pyrrolidine-2,5-dioneHCID 2183483883%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of succinic anhydride (250 mg, 2.50 mmol) and 4-amino-4′-chloro diphenylether (500 mg, 2.27 mml) in toluene is heated to 110° C. for 14 h. and cooled down to room temperature. SOCl2 (1.5 mL) is added into the mixture and stirred at room temperature for 8 h. After the solvent is removed under vacuum, the residue is treated with saturated NaHCO3 aqueous solution (20 mL) and extracted with CHCl3 (3×50 mL). The combined organic layer is washed with brine and dried (MgSO4). After filtering the drying agent, the filtrate is concentrated and purified by flash column chromatography (silica gel, EtOAc/hexane 30%˜80%) to provide 1-[4-(4-chloro-phenoxy)-phenyl]-pyrrolidine-2,5-dione as white solid (570 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431607B2
Source datasetuspto-grants-2013_04
ORD IDord-27372413f40c435287ff7bf4b98e13d5
Source noteuspto-grants-2013_04