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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132589생성일: 2026년 10월 26일

2-Nitrophenol → 1-(Benzhydryloxy)-2-nitrobenzene

https://huagongshe.com/reaction/132589

반응식

참여 물질

역할이름HCID투입량
반응물2-NitrophenolHCID 6947—
반응물Potassium CarbonateHCID 11430—
반응물BromodiphenylmethaneHCID 236603—
반응물PotassiumHCID 5462222—
용매AcetoneHCID 180—
생성물1-(Benzhydryloxy)-2-nitrobenzeneHCID 743412239.5%

반응 단계

A mixture of o-nitrophenol (2.08 g, 15.0 mmol), 1-[bromo(phenyl)methyl]benzene (3.70 g, 15.0 mmol) and potassium carbonated (K2CO3) (4.14 g, 30.0 mmol) in acetone (60 mL) was kept at reflux temperature for 5 h. The reaction mixture was cooled to room temperature, concentrated in vacuo. The residue was partitioned between dichloromethane (CH2Cl2) and water (H2O), organic layer dried over sodium sulphate (Na2SO4), filtered, concentrated. The residue was purified by silica gel flash chromatography to give subtitled compound (1.81 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388020B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-079031298525448db5b6e52e03b4a7e2
출처 메모uspto-grants-2008_06