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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45524생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/45524

반응식

참여 물질

역할이름HCID투입량
반응물N-(2-Hydroxyethyl)phthalimideHCID 77499—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물(4-Bromophenyl)(4-chlorophenyl)methanolHCID 57659206—
용매TolueneHCID 1140—
생성물2-{2-[(4-Bromo-phenyl)-(4-chloro-phenyl)-methoxy]-ethyl}-isoindole-1,3-dioneHCID 5933192256.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541461B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-02b2cacfa25c40dc8ae5eae96b3f27ec
출처 메모uspto-grants-2013_09