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HRID 45524作成日:2026年10月25日

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

https://huagongshe.com/reaction/45524

反応式

関与物質

役割名称HCID仕込み量
反応物N-(2-Hydroxyethyl)phthalimideHCID 77499—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物(4-Bromophenyl)(4-chlorophenyl)methanolHCID 57659206—
溶媒TolueneHCID 1140—
生成物2-{2-[(4-Bromo-phenyl)-(4-chloro-phenyl)-methoxy]-ethyl}-isoindole-1,3-dioneHCID 5933192256.3%

反応手順

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-toluenesulfonic 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541461B2
出典データセットuspto-grants-2013_09
ORD IDord-02b2cacfa25c40dc8ae5eae96b3f27ec
出典メモuspto-grants-2013_09