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ChemicalBook CAS DataBase List 4,4'-Diaminobenzanilide

4,4'-Diaminobenzanilide synthesis

6synthesis methods
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Yield:785-30-8 96.1%

Reaction Conditions:

Stage #1:4,4'-dinitrobenzanilide with palladium on activated charcoal;hydrogen in N,N-dimethyl-formamide at 10; under 6000.6 Torr;Autoclave;
Stage #2: in butan-1-ol at 25 - 135; for 0.333333 h;Autoclave;

Steps:

4 The preparation method of the electronic grade 4,4'-diaminobenzanilide of this embodiment has the following steps
2 To the autoclave, 30 g of 4,4'-dinitrobenzanilide obtained in step 1, 150 mL of N,N'-dimethylformamide, and 0.8 g of a 3 wt% palladium carbon catalyst were added. Into the hydrogen,The pressure-holding reaction was completed to completion at a pressure of 0.8 ± 0.1 MPa and a temperature of 100 ± 1 °C.After completion of the reaction, the mixture was filtered, and the solvent was evaporated to vacuo.The crude 4,4'-diaminobenzanilide was obtained.3 The crude 4,4'-diaminobenzanilide obtained in the step 2 was further added to the autoclave, 100 g of n-butanol and 0.96 g of activated carbon were added, and the nitrogen was replaced three times, and the nitrogen gas was discharged until the inside of the autoclave was maintained at a positive pressure.Then, the temperature was raised to 135±1° C., stirred for 20 min, filtered under nitrogen, and the filtrate was cooled to 25±1° C., filtered, and dried.22.8 g of an electronic grade 4,4'-diaminobenzanilide having a white crystalline powder was obtained in a yield of 96.1% and a purity of 99.7% (HPLC).

References:

Jiangsu Shang Laite Pharmaceutical And Chemical Materials Co., Ltd.;Hu Guoyi;Hu Jinping;Wu Jianhua;Zhang Peifeng;Xi Xiaojin CN108329224, 2018, A Location in patent:Paragraph 0013; 0015-0017; 0026; 0028-0030

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