戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 897465作成日:2026年10月24日

Water → 5-Bromo-2-phenoxypyrimidine

https://huagongshe.com/ja/reaction/897465

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PhenolHCID 996—
反応物Potassium HydroxideHCID 14797—
反応物5-Bromo-2-chloropyrimidineHCID 606665—
触媒Dibenzo-18-crown-6HCID 26541—
溶媒TolueneHCID 1140—
生成物5-Bromo-2-phenoxypyrimidineHCID 64284254.4%

反応手順

A mixture of 5-bromo-2-chloropyrimidine (5.00 g, 0.0259 mol), phenol (3.16 g, 0.0336 mol), dibenzo-18-Crown-6 (0.47 g, 0.0013 mol) and ground potassium hydroxide (3.51 g, 0.0626 mol) in toluene (75 ml) was heated at reflux for 5 hours with azeotropic removal of water. The mixture was allowed to cool to ambient temperature and the solvent was removed under reduced pressure. The residue was partitioned between water and chloroform. The layers were separated and the aqueous phase was extracted with chloroform three times. The combined organic layers were dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography on silica using n-heptane/ethyl acetate (98:2) as an eluent to give 5-bromo-2-phenoxy-pyrimidine as a white solid (3.55 g, 0.0141 mol): 1H NMR (DMSO-d6, 400 MHz) 8.80 (s, 2H), 7.45 (t, 2H), 7.27 (t, 1H), 7.22 (d 2H); TLC (n-heptane/ethyl acetate=95:5) Rf 0.20.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06921763B2
出典データセットuspto-grants-2005_07
ORD IDord-ece28418e4614288bf5fd0fd7c32b5ee
出典メモuspto-grants-2005_07