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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 909285생성일: 2026년 10월 27일

Ethyl Acetate → Methyl 2-(2-benzyloxyphenyl)-5-nitrobenzoate

https://huagongshe.com/reaction/909285

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참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Cesium carbonateHCID 10796—
반응물Methyl 2-Bromo-5-nitrobenzoateHCID 245494—
반응물(2-(Benzyloxy)phenyl)boronic acidHCID 2773253—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물Methyl 2-(2-benzyloxyphenyl)-5-nitrobenzoateHCID 5802686865.2%

반응 조건

온도80 °C

반응 단계

A mixture of 2-benzyloxyphenylboronic acid (20.2 g, 88.6 mmol), methyl 2-bromo-5-nitrobenzoate (25.4 g, 97.5 mmol), cesium carbonate (57.7 g, 177 mmol) and bis(triphenylphosphine)palladium(II) dichloride (1.16 g, 1.65 mmol) was suspended in anhydrous N,N-dimethylformamide (300 mL), and then was stirred under argon atmosphere at 80° C. for 3 days. After cooling down, ethyl acetate (500 mL), diethylether (300 mL) and water (500 mL) were added thereto, and then separated. The aqueous layer was extracted with a mixture of ethyl acetate (200 mL) and diethylether (200 mL). The combined organic layer was washed with water (500 mL, twice) and saturated brine (300 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (21.0 g) as a pale yellow oil. (Yield 65%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08017775B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-2977104239f344e7ab4df5fc76f21ad5
출처 메모uspto-grants-2011_09