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HRID 27379作成日:2026年10月25日

4-Chloro-3-nitrobenzophenone → {4-[Methyl(octyl)amino]-3-nitrophenyl}(phenyl)methanone

https://huagongshe.com/reaction/27379

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-3-nitrobenzophenoneHCID 41743—
反応物OctylmethylamineHCID 75538—
溶媒EthanolHCID 702—
生成物{4-[Methyl(octyl)amino]-3-nitrophenyl}(phenyl)methanoneHCID 23342777—

反応手順

A mixture of 9.23 g. of 3-nitro-4-chloro-benzophenone, 10 ml. of ethanol and 10.3 g. of N-methyl-N-octylamine is stirred at 80° to 85° C. for 30 minutes, and then the mixture is poured onto 100 ml. of ice water. The aqueous phase is extracted with 2×75 ml. of benzene. The benzene phases are combined, washed with distilled water until chloride-free, dried over anhydrous magnesium sulphate, filtered, and evaporated in vacuo. 11.57 g. of 3-nitro-4-(N-methyl-N-octylamino)-benzophenone are obtained in the form of an oily residue. On the basis of thin layer chromatographical examination, a pure, uniform product is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04221739
出典データセットuspto-grants-1980_09
ORD IDord-f293bf93d94348b09e6e14922f208abc
出典メモuspto-grants-1980_09