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HRID 1719638作成日:2026年10月27日

Ammonia → Benzenamine, 3-((4-aminophenyl)methyl)-

https://huagongshe.com/reaction/1719638

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物(4-Chloro-3-nitrophenyl)(4-nitrophenyl)methanoneHCID 554735—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒Glycol monoethyl etherHCID 8076—
生成物Benzenamine, 3-((4-aminophenyl)methyl)-HCID 146674—

反応手順

15.3 g (0.05 mol) of 3,4'-dinitro-4-chlorobenzophenone, 0.75 g of 5% Pd/C and 50 ml of ethyl cellosolve were charged in a closed glass vessel equipped with a thermometer and a stirrer. While stirring the mixture at a temperature of 75° to 80° C., hydrogen was introduced thereinto and 10.3 l (0.46 mol) of hydrogen was absorbed in 13 hours. Since no more absorption of hydrogen was observed, the reaction was terminated at this point. The reaction solution was neutralized with 3.6 g (0.06 mol) of 28% aqueous ammonia. The catalyst was removed by filtration. The filtrate was concentrated to obtain 3,4'-diaminodiphenylmethane as a brown oil. A high performance liquid chromatography revealed that the purity was 88.2%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04540818
出典データセットuspto-grants-1985_09
ORD IDord-c5bfde3dbf194434ab83be76cf615e33
出典メモuspto-grants-1985_09