Реакция #932

ord-8c04216a28bb4609b9208e0d1a14c091

Уравнение реакции

Cc1cc(C)cc(Sc2cccc([N+](=O)[O-])c2C#N)c1
2-[(3,5-Dimethylphenyl)thio]-6-nitrobenzonitrile
Cc1cc(C)cc(Sc2cccc([N+](=O)[O-])c2C#N)c1
2-[(3,5-dimethylphenyl)thio]-6-nitrobenzonitrile
[Na+].[OH-]
NaOH
Cc1cc(C)cc(Sc2cccc(N)c2C#N)c1
2-amino-6-[(3,5-dimethylphenyl)thio]benzonitrile
Выход 64.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGAfter stirring 1 h and 15 min
  2. 2
    workup.ADDITIONadded
  3. 3
    workup.STIRRINGThe mixture was stirred for 1 h
  4. 4
    Фильтрацияthe solid was collected by vacuum filtration

Методика

2-[(3,5-Dimethylphenyl)thio]-6-nitrobenzonitrile (Example 5) (1.0 g, 0.0035 mol) was dissolved in 50 ml of diglyme. A solution of stannous chloride-2H2O (3.16 g, 0.014 mol) in 15 ml of concentrated HCl was added dropwise with stirring. After stirring 1 h and 15 min, the reaction mixture was poured into a solution of 12 g NaOH in 100 ml of water with ice added to bring the total volume to 300 ml. The mixture was stirred for 1 h and the solid was collected by vacuum filtration. Chromatography on silica gel (flash; Hex/EtOAc 1:1) provided 0.57 g (64%) of 2-amino-6-[(3,5-dimethylphenyl)thio]benzonitrile: mp 124°-125° C.; NMR (Me2SO-d6, 300 MHz) δ 2.23 (s, H), 6.17 (br, 2H), 6.24 (apparent d, 1H), 7.00 (m, 3H), 7.09 (apparent t, 1H); mass spec (CI) 255 (M+ +1, 100%). Anal. Calc. for C15H14N2S: C, 70.83; H, 5.55; N, 11.01; S, 12.61. Found: C, 70.84; H, 5.60; N, 10.98; S, 12.53.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723452uspto-grants-1998_03