戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 471978作成日:2026年10月24日

2-Bromo-5-nitroanisole → 2-Bromo-5-nitrophenol

https://huagongshe.com/ja/reaction/471978

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-5-nitroanisoleHCID 101293—
反応物Pyridinium chlorideHCID 10176127—
反応物2-Methoxy-4-nitro-1-(trifluoromethyl)benzeneHCID 17755961—
生成物2-Bromo-5-nitrophenolHCID 12867136—
生成物5-Nitro-2-(trifluoromethyl)phenolHCID 21959586—

反応条件

温度210 °C

反応手順

To a mixture of 2-methoxy-4-nitro-1-(trifluoromethyl)benzene and 1-bromo-2-methoxy-4-nitro-benzene (16 g, crude) was added pyridine hydrochloride (100 g, 860 mmol) and the reaction mixture was stirred at 210° C. for 40 min. Then the mixture was poured into ice-water and extracted with EtOAc (80 mL×3). The combined organic layers were washed with water (100 mL×2) and brine (50 mL), dried over anhydrous Na2SO4 and purified by silica gel column chromatography (5% EtOAc in petroleum as eluant) to afford 5-nitro-2-(trifluoromethyl)phenol and 2-bromo-5-nitrophenol (10 g, crude). 1H-NMR (300 MHz, CDCl3) δ 7.86-7.80 (m, 3H), 7.72-7.63 (m, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633189B2
出典データセットuspto-grants-2014_01
ORD IDord-8d889ff695d346a89f062978fd9bd2db
出典メモuspto-grants-2014_01