【结 构 式】 |
【分子编号】23810 【品名】1-(4-fluoro-2-hydroxyphenyl)-1-ethanone 【CA登记号】1481-27-2 |
【 分 子 式 】C8H7FO2 【 分 子 量 】154.1407832 【元素组成】C 62.34% H 4.58% F 12.33% O 20.76% |
与该中间体有关的原料药合成路线共 1 条
合成路线1
该中间体在本合成路线中的序号:(II)Friedel-Crafts acylation of 3-fluorophenol (I) with acetic anhydride in the presence of AlCl3 at 120 C provided 4-fluoro-2-hydroxy-acetophenone (II). Subsequent treatment of (II) with phthaloyl chloride (III) in pyridine afforded diester (IV). Heating of (IV) with K2CO3 in pyridine, followed by acidic work-up yielded the title flavone.
【1】 Belluti, F.; Carrara, M.; Rampa, A.; Gobbi, S.; Da Re, P.; Valenti, P.; Cima, L.; Bisi, A.; Synthesis of flavone-2'-carboxylic acid analogues. Anti-Cancer Drug Des 1998, 13, 8, 881. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(I) | 23809 | 3-fluorophenol | 372-20-3 | C6H5FO | 详情 | 详情 |
(II) | 23810 | 1-(4-fluoro-2-hydroxyphenyl)-1-ethanone | 1481-27-2 | C8H7FO2 | 详情 | 详情 |
(III) | 23811 | phthaloyl dichloride;1,2-Benzenedicarbonyl dichloride;o-Phthaloyl chloride | 88-95-9 | C8H4Cl2O2 | 详情 | 详情 |
(IV) | 23812 | bis(2-acetyl-5-fluorophenyl) phthalate | C24H16F2O6 | 详情 | 详情 |
Extended Information