Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-(2-Hydroxyethyl)phthalimide → 2-{2-[(4-Bromo-phenyl)-(4-chloro-phenyl)-methoxy]-ethyl}-isoindole-1,3-dione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-(2-Hydroxyethyl)phthalimide | HCID 77499 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 반응물 | (4-Bromophenyl)(4-chlorophenyl)methanol | HCID 57659206 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-{2-[(4-Bromo-phenyl)-(4-chloro-phenyl)-methoxy]-ethyl}-isoindole-1,3-dione | HCID 59331922 | 56.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08541461B2 |
| 출처 데이터셋 | uspto-grants-2013_09 |
| ORD ID | ord-02b2cacfa25c40dc8ae5eae96b3f27ec |
| 출처 메모 | uspto-grants-2013_09 |