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HRID 1160生成日期:2026年10月23日

乙醇 → 2-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidine

https://huagongshe.com/zh-CN/reaction/1160

反应方程式

参与物

角色名称HCID投料
反应物乙醇HCID 702—
反应物三氯甲烷HCID 6212—
反应物硼氢化钠HCID 4311764—
反应物2-(4-Acetylphenyl)-5-decyloxypyrimidineHCID 19694901—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
产物2-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidineHCID 21468280100.3%

反应步骤

35.5 g (0.1 mo1) of 2-(4-acetylphenyl)-5-decyloxypyrimidine, 300 ml of ethanol and 300 ml of chloroform were supplied into a four-necked flask equipped with a stirrer and a thermometer. Then 2.8 g (0.075 mol) of sodium borohydride was added at 30°-40° C. and the mixture was stirred at the same temperature for 4 hours. The resulting reaction mixture was poured into 500 ml of water, followed by extraction and liquid separation, and the obtained chloroform layer was washed with water, then dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 35.8 g of 2-(4-(1-hydroxyethyl) phenyl)-5-decyloxypyrimidine (II-c-11) (yield: 100%).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05723610
来源数据集uspto-grants-1998_03
ORD IDord-8266c5cd4a68414b8c3137da7bc01eef
来源说明uspto-grants-1998_03