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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924733Generated: 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/924733

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 numberUS09283226B2
Source datasetuspto-grants-2016_03
ORD IDord-695ba2828ac8472aa7459e6eb89cf3b8
Source noteuspto-grants-2016_03