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4-Chloro-3-nitrobenzophenone → {4-[Methyl(octyl)amino]-3-nitrophenyl}(phenyl)methanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Chloro-3-nitrobenzophenone | HCID 41743 | — |
| 反応物 | Octylmethylamine | HCID 75538 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | {4-[Methyl(octyl)amino]-3-nitrophenyl}(phenyl)methanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04221739 |
| 出典データセット | uspto-grants-1980_09 |
| ORD ID | ord-f293bf93d94348b09e6e14922f208abc |
| 出典メモ | uspto-grants-1980_09 |