Реакция #2195489

ord-22c274b5414341ad8bef442990382bc3

Уравнение реакции

Cn1c(=O)oc(=O)c2ccccc21
N-methylisatoic anhydride
Cl
HCl
CCOC(=O)C[N+](=O)[O-]
ethylnitroacetate
[H-].[Na+]
sodium hydride
[H][H]
hydrogen
Cn1c(=O)c([N+](=O)[O-])c(O)c2ccccc21
yellow solids
Выход 27.0%
Cn1c(=O)c([N+](=O)[O-])c(O)c2ccccc21
4-Hydroxy-1-methyl-3-nitro-1H-quinolin-2-one
Выход 27.0%

Растворители

Условия реакции

Температура
90°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураcooled to room temperature
  2. 2
    Температураheated overnight at 120° C
  3. 3
    ТемператураThe mixture was cooled to room temperature
  4. 4
    ДругоеThe solids formed
  5. 5
    Фильтрацияwere filtered
  6. 6
    Промывкаwashed several times by water

Методика

A solution of ethylnitroacetate (15.96 g, 120 mmol) was added slowly in a suspension of sodium hydride (60% in mineral oil, 5.28 g, 132 mmol) in dimethylacetamide under N2 atmosphere. The mixture was allowed to stir at room temperature until the evolution of hydrogen gas ceased, then heated to 90° C. for 30 min. and cooled to room temperature. A solution of N-methylisatoic anhydride (23.38 g, 132 mmol) in dimethylacetamide was added slowly and heated overnight at 120° C. The mixture was cooled to room temperature, poured into ice water, and acidified by cold 10% HCl. The solids formed were filtered and washed several times by water to yield 7.1 g (27%) of yellow solids. Mp 193° C. 1H NMR (DMSO-d6): δ 3.60 (s, 3H), 7.37 (t, J=7.6 Hz, 1H), 7.58 (d, J=8.5 Hz, 1H), 7.77 (t, J=7.5 Hz, 1H), 8.12 (d, J=7.9 Hz, 1H). EIMS m/z 221 (M+1), 243 (M+23). Anal. (C10H8N2O4) C, H, N.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07514225B2uspto-grants-2009_04