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乙醇 → 2-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidine
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-decyloxypyrimidine | HCID 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-decyloxypyrimidine | HCID 21468280 | 100.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 专利号 | US05723610 |
| 来源数据集 | uspto-grants-1998_03 |
| ORD ID | ord-8266c5cd4a68414b8c3137da7bc01eef |
| 来源说明 | uspto-grants-1998_03 |