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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361798Generated: October 26, 2026

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

https://huagongshe.com/reaction/2361798

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) Rt 4.07 no observable mass ion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691806B2
Source datasetuspto-grants-2014_04
ORD IDord-504a0034a29246ffb1769bf0d852b536
Source noteuspto-grants-2014_04