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HRID 461626作成日:2026年10月26日

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

https://huagongshe.com/reaction/461626

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 2x75 ml. of benzene. The benzene phases are combined, washed with distilled water with 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US04064121
出典データセットuspto-grants-1977_12
ORD IDord-5008c09bbebb4d06a7beba95648bd188
出典メモuspto-grants-1977_12