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【结 构 式】

【分子编号】59706

【品名】(2-chloro-5-nitrophenyl)(4-methoxyphenyl)methanone

【CA登记号】

【 分 子 式 】C14H10ClNO4

【 分 子 量 】291.69044

【元素组成】C 57.65% H 3.46% Cl 12.15% N 4.8% O 21.94%

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:(III)

Treatment of 2-chloro-5-nitrobenzoic acid (I) with PCl5 provides acid chloride (II), which is then condensed with anisole in the presence of AlCl3 to furnish the benzophenone (III). Alternatively, ketone (III) is prepared by Friedel-Crafts condensation of 2-chloro-5-nitrobenzoic acid (I) with anisole in hot polyphosphoric acid. Reduction of ketone (III) employing triethylsilane and trifluoromethanesulfonic acid gives rise to diphenylmethane derivative (IV)

1 Manning, R.E.; Tremont, S.J.; Glenn, K.C.; Keller, B.T. (Pharmacia Corp.); Combination therapy for the prophylaxis and treatment of hyperlipidemic conditions and disorders. WO 0168096 .
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) 10188 2-Chloro-5-nitrobenzoic acid 2516-96-3 C7H4ClNO4 详情 详情
(II) 10189 2-Chloro-5-nitrobenzoyl chloride 25784-91-2 C7H3Cl2NO3 详情 详情
(III) 59706 (2-chloro-5-nitrophenyl)(4-methoxyphenyl)methanone C14H10ClNO4 详情 详情
(IV) 59707 4-(2-chloro-5-nitrobenzyl)phenyl methyl ether; 1-chloro-2-(4-methoxybenzyl)-4-nitrobenzene C14H12ClNO3 详情 详情
Extended Information