戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 402785作成日:2026年10月25日

Cesium carbonate → 4-Bromo-2-chloro-1-[(3-methylbut-3-en-1-yl)oxy]benzene

https://huagongshe.com/reaction/402785

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-Bromo-2-chlorophenolHCID 19859—
反応物3-Methylbut-3-en-1-yl diphenyl phosphateHCID 12280977—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-Bromo-2-chloro-1-[(3-methylbut-3-en-1-yl)oxy]benzeneHCID 66764573—

反応条件

温度85 °C

反応手順

To a mixture of 4-bromo-2-chlorophenol (0.98 g, 4.71 mmol), and Cs2CO3 (2.05 g, 6.28 mmol) in DMF (4.49 mL) at room temperature was added 3-methylbut-3-en-1-yl diphenyl phosphate (1.00 g, 3.14 mmol, synthesized according to a procedure in U.S. Pat. No. 5,006,550, 9 Apr. 1991) dropwise via a syringe. The reaction mixture was heated to 85° C. for 1 hour. It was then allowed to cool to room temperature and was diluted with water (20.0 mL). The resulting mixture was extracted with hexane (75.0 mL, 2×) and the combined organic layers were dried over Na2SO4, filtered, and concentrated under vacuum. The crude mixture was purified by silica gel chromatography eluting with 0-5% EtOAc/hexanes to give the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742110B2
出典データセットuspto-grants-2014_06
ORD IDord-b6f475f2bd914eabb6253a1e73646b72
出典メモuspto-grants-2014_06