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【结 构 式】

【分子编号】34018

【品名】(4-fluorophenyl)(2-thienyl)methanone

【CA登记号】579-49-7

【 分 子 式 】C11H7FOS

【 分 子 量 】206.2403832

【元素组成】C 64.06% H 3.42% F 9.21% O 7.76% S 15.55%

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)

The reaction of 2-thiophenecarbonyl chloride (I) with fluorobenzene (A) by means of AlCl3 gives (4-fluorophenyl)(2-thienyl)ketone (II), which is then condensed with diethyl methylmalonate (B) by means of NaH in benzene-HMPA to yield diethyl 2-methyl-2-[4-(2-thienylcarbonyl)phenyl]malonate (III); this product is finally hydrolyzed and partially decarboxylated with refluxing aqueous NaOH.

1 Van Daele, P.G.H.; et al.; Synthesis of alpha-methyl-4-(2-thienylcarbonyl)benzene acetic acid, suprofen and derivatives. Arzneim-Forsch Drug Res 1975, 25, 10, 1495-1501.
2 Castaner, J.; Chatterjee, S.S.; Suprofen. Drugs Fut 1976, 1, 3, 148.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(A) 17466 Fluorobenzene 462-06-6 C6H5F 详情 详情
(B) 30310 diethyl 2-methylmalonate 609-08-5 C8H14O4 详情 详情
(I) 14103 2-Thiophenecarbonyl chloride 5271-67-0 C5H3ClOS 详情 详情
(II) 34018 (4-fluorophenyl)(2-thienyl)methanone 579-49-7 C11H7FOS 详情 详情
(III) 34019 diethyl 2-methyl-2-[4-(2-thienylcarbonyl)phenyl]malonate C19H20O5S 详情 详情
Extended Information