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HRID 1360039作成日:2026年10月24日

4-Iodophenol → 2-(4-Iodophenoxy)-4,6-dimethylpyrimidine

https://huagongshe.com/ja/reaction/1360039

反応式

関与物質

役割名称HCID仕込み量
反応物4-IodophenolHCID 10894—
反応物2-Chloro-4,6-dimethylpyrimidineHCID 20550—
反応物Sodium hydrideHCID 24758—
生成物2-(4-Iodophenoxy)-4,6-dimethylpyrimidineHCID 5776249768.4%

反応手順

Under an argon atmosphere, phosphorus oxychloride (2 ml) was added to 4,6-dimethyl-2-hydroxypyrimidine (400 mg), and the resulting mixture was stirred for 1 hour while heating the mixture to reflux. The reaction solution was cooled to room temperature, and the cooled solution was added in small portions to water. After adding sodium hydrogen carbonate in small portions to the resulting mixture to neutralize it, the mixture was extracted with ethyl acetate. Organic layer was washed twice with water and once with saturated brine, and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated to obtain 2-chloro-4,6-dimethylpyrimidine (350 mg). (2) In the same manner as in Reference Example 8, 4-iodophenol (223 mg) and 2-chloro-4,6-dimethylpyrimidine (157 mg) were reacted by using sodium hydride to obtain 2-(4-iodophenoxy)-4,6-dimethylpyrimidine (226 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07879837B2
出典データセットuspto-grants-2011_02
ORD IDord-a1a8f4f815514301b7495aa3c141c5a6
出典メモuspto-grants-2011_02