Реакция #159268

ord-333ac6e4e9aa4208bd8f5b2a462024ad

Уравнение реакции

O=[N+]([O-])c1ccc(Br)cc1
4-nitro-bromobenzene
CC(=O)c1ccc(B(O)O)cc1
4-acetylphenyl boronic acid
CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
4′-nitro-4-acetylbiphenyl
Выход 97.0%

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеmp 144-146° C. (lit.,7 150-151° C.)

Методика

From 4-nitro-bromobenzene and 4-acetylphenyl boronic acid, yield 97%; mp 144-146° C. (lit.,7 150-151° C.); IR: 1681, 1530, 1497, 1361 and 1280; 1H NMR (400 MHz; CDCl3): 8.02 (2H, d, J 8.5), 7.64-7.56 (4H, m), 7.16 (2H, t, J 8.5) and 2.63 (3H, s); 13C NMR (CDCl3): 197.5, 164.2, 144.7, 136, 128.9, 127, 116, 115.7 and 26.6; m/z (EI) 199 (30%, M+−C2H2O), 131 (50) and 69 (100)(Found: M+−C2H2O, 199.062).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08828902B2uspto-grants-2014_09