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HRID 480655作成日:2026年10月26日

Boron tribromide → 3-Fluoro-4-methylphenol

https://huagongshe.com/reaction/480655

反応式

関与物質

役割名称HCID仕込み量
反応物Boron tribromideHCID 25134—
反応物3-Fluoro-4-methylanisoleHCID 2774571—
溶媒DichloromethaneHCID 6344—
生成物3-Fluoro-4-methylphenolHCID 277461375.2%

反応条件

温度-70 °C

反応手順

To a −70° C. solution of 3-fluoro-4-methyl anisole (1.62 g; 11.6 mmol) in CH2Cl2 (10 mL) was added dropwise BBr3 (10 mL; 12 mmol). The reaction mixture was stirred at −70° C. for 10 min, then allowed to warm to 0° C. and stirred at 0° C. for 2 h. The reaction was allowed to warm to RT and concentrated in vacuo and the residue was partitioned between H2O and EtOAc. The organic phase was washed with H2O, dried (Na2SO4) and concentrated in vacuo to give 3-fluoro-4-methyl phenol (1.1 g; 75%) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06653314B2
出典データセットuspto-grants-2003_11
ORD IDord-773cb28411f74f21b62a1ac81b99ead0
出典メモuspto-grants-2003_11