戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 132589作成日:2026年10月26日

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

https://huagongshe.com/reaction/132589

反応式

関与物質

役割名称HCID仕込み量
反応物2-NitrophenolHCID 6947—
反応物Potassium CarbonateHCID 11430—
反応物BromodiphenylmethaneHCID 236603—
反応物PotassiumHCID 5462222—
溶媒AcetoneHCID 180—
生成物1-(Benzhydryloxy)-2-nitrobenzeneHCID 743412239.5%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07388020B2
出典データセットuspto-grants-2008_06
ORD IDord-079031298525448db5b6e52e03b4a7e2
出典メモuspto-grants-2008_06