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ChemicalBook CAS DataBase List 3-AMINOBIPHENYL
2243-47-2

3-AMINOBIPHENYL synthesis

14synthesis methods
Dissolve p-hydroxybiphenyl in methyl tert-butyl ether, mixing and stirring well, drop nitric acid into the resulting mixed solution, continue stirring for 1-3h after dropping, and the temperature of the whole process is controlled at 20-40℃; obtain the so
-

Yield:2243-47-2 98%

Reaction Conditions:

with chloro[(di(1-adamantyl)-N-butylphosphine)-2-(2-aminobiphenyl)]palladium(II);potassium carbonate in N,N-dimethyl-formamide at 80;Inert atmosphere;

Steps:

3 3-amino-biphenyl preparation
Under nitrogen, 1L four-mouth bottle, mechanical stirring, adding 500mLN, N-dimethyl formamide (DMF), 50g3-aminochlorobenzene, 57.3g phenyltheophylline boric acid, 108.4g potassium carbonate, 0.26g palladium catalyst 2GAd2 (n-bu) PPd (Chloro [(di (1-adamantyl)-N-butylphosphine) - 2 - (2-aminobiphenyl)] palladium (II)), in 80 °C reaction sleepovers. Plus 20g naoh 100 ml aqueous solution quenching, 300 ml ethyl acetate extraction, the organic phase exsolution, to obtain crystal micro purple 3-aminobiphenyl 65g, the yield is 98%.

References:

Beijing Greenchem Technology Co., Ltd.;Rao, Zhihua;Gong, Ningrui CN105439871, 2016, A Location in patent:Paragraph 0076; 0077; 0078; 0079

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