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2-Nitrophenol → 1-(Benzhydryloxy)-2-nitrobenzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Nitrophenol | HCID 6947 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Bromodiphenylmethane | HCID 236603 | — |
| 反応物 | Potassium | HCID 5462222 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 1-(Benzhydryloxy)-2-nitrobenzene | HCID 7434122 | 39.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07388020B2 |
| 出典データセット | uspto-grants-2008_06 |
| ORD ID | ord-079031298525448db5b6e52e03b4a7e2 |
| 出典メモ | uspto-grants-2008_06 |