戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 56545作成日:2026年10月24日

Potassium Hydroxide → 5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene

https://huagongshe.com/ja/reaction/56545

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物Bromodifluoromethyl diethylphosphonateHCID 144101—
反応物4-Bromo-2,6-dimethoxyphenolHCID 14845876—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzeneHCID 5843207162%

反応条件

温度-78 °C

反応手順

5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene was synthesized from 4-bromo-2,6-dimethoxyphenol according to the procedure of Zafrani, Y. Tetrahedron 2009, 65, 5278 as follows. To a solution of 4-bromo-2,6-dimethoxyphenol (1.08 g, 4.6 mmol) in MeCN (27 mL) was added a solution of KOH (5.0 g, 89 mmol) in H2O (27 mL). The mixture was immediately cooled over a −78° C. bath and diethyl(bromodifluoromethyl)phosphonate (1.6 mL, 8.9 mmol) was added. The flask was sealed with a septum and the cold bath was removed. The mixture was stirred for a total of 3.5 hrs during which time the septum was ejected from the flask. The reaction was diluted with EtOAc and the layers were separated. The aqueous layer was extracted with EtOAc and the combined organics were washed with 1 M NaOH, H2O and brine then dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (0-30% EtOAc-hexanes) provided 5-bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene as a white solid (0.808 g, 62% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434707B2
出典データセットuspto-grants-2016_09
ORD IDord-11df3402760d45b2a0c38bdeab5e3b2c
出典メモuspto-grants-2016_09