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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888596Generated: October 27, 2026

N-(2-Hydroxyethyl)phthalimide → 2-{2-[(4-Bromo-phenyl)-(4-chloro-phenyl)-methoxy]-ethyl}-isoindole-1,3-dione

https://huagongshe.com/reaction/888596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Hydroxyethyl)phthalimideHCID 77499—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant(4-Bromophenyl)(4-chlorophenyl)methanolHCID 57659206—
SolventTolueneHCID 1140—
Product2-{2-[(4-Bromo-phenyl)-(4-chloro-phenyl)-methoxy]-ethyl}-isoindole-1,3-dioneHCID 5933192256.3%

Reaction Steps

A mixture of (4-Bromo-phenyl)-(4-chloro-phenyl)-methanol (2.3 g, 7.73 mmol), N-(2-hydroxyethyl)phthalimide (1.4 g, 7.36 mmol) and para-toluenesulphonic acid monohydrate (560 mg, 2.94 mmol) in toluene (50 ml) was heated to reflux under Dean-Stark conditions for 17 hours. Upon cooling, the solvent was removed and the residue was partitioned between ethyl acetate and water. The organic layer was then dried (MgSO4), filtered and concentrated. The crude product was purified by column chromatography (SiO2), eluting with ethyl acetate/petroleum ether (1:4), to yield the title compound (1.95 g). LC/MS: (PS-B3) R1 4.07 no observable mass ion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247576B2
Source datasetuspto-grants-2012_08
ORD IDord-ba424da7aab54723850ac71300d94124
Source noteuspto-grants-2012_08