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HRID 29231作成日:2026年10月24日

Methanol → 4-Bromo-2-methoxybenzonitrile

https://huagongshe.com/ja/reaction/29231

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物DichloromethaneHCID 6344—
反応物Potassium CarbonateHCID 11430—
反応物4-Bromo-2-fluorobenzonitrileHCID 736029—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物4-Bromo-2-methoxybenzonitrileHCID 2234670295.6%

反応条件

温度55 °C

反応手順

A mixture of 4-bromo-2-fluoro-benzonitrile (15.0 g, 75.0 mmol), methanol (30.4 mL, 350 mmol) and potassium carbonate (31.1 g, 225 mmol) in DMF (150 mL) was stirred under argon at 55° C. overnight. At this point TLC (100% methylene chloride) revealed no starting material, and the reaction mixture was poured into ether (300 mL) and water (150 mL). The layers were separated, and the organic layer was washed with water (150 mL) and brine (50 mL), dried over Mg2SO4, filtrated, and concentrated under reduced pressure, providing (15.2 g, 95.5%) of 4-bromo-2-methoxy-benzonitrile as a white solid. 1H-NMR (CDCl3) δ 7.41 (d, J=8.1 Hz, 1H), 7.16 (dd, J=8.1, 1.6 Hz, 1H), 7.13 (d, J=1.6 Hz, 1H), 3.93 (s, 3H); MS GC-MS (M+=211; RT=6.15 min).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420066B2
出典データセットuspto-grants-2008_09
ORD IDord-dfe0619ae872459c9e0030ceb8e4fcb6
出典メモuspto-grants-2008_09