反応 #2195493

ord-b77a5f7ad4514b0892c2b3a583c08a22

反応方程式

O=c1[nH]c2ccccc2c(=O)o1
isatoic anhydride
CC(=O)N(C)C
dimethylacetamide
Cl
HCl
CCC(CC)(C(=O)[O-])C(=O)[O-]
diethylmalonate
[H-].[Na+]
sodium hydride
CC(=O)N(C)C
dimethylacetamide
[H][H]
hydrogen
CCOC(=O)c1c(O)c2ccccc2[nH]c1=O
white solids
収率 47.0%
CCOC(=O)c1c(O)c2ccccc2[nH]c1=O
4-Hydroxy-2-oxo-1,2-dihydro-quinoline-3-carboxylic acid ethyl ester
収率 47.0%

反応条件

温度
90°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled to room temperature
  2. 2
    温度heated at 120° C. for 15 h
  3. 3
    温度The mixture was cooled to room temperature
  4. 4
    その他The solids formed
  5. 5
    ろ過were filtered
  6. 6
    洗浄washed several times by water

実験手順

A solution of diethylmalonate (80 g, 0.50 mol) was added slowly to a suspension of sodium hydride (60% in mineral oil, 22 g, 0.55 mol) 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 isatoic anhydride (89.72 g, 0.55 mmol) in dimethylacetamide was added slowly and heated at 120° C. for 15 h. 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 55 g (47%) of white solids. Mp 173° C. 1H NMR (DMSO-d6): δ 1.30 (t, J=6.9 Hz, 3H), 4.33 (q, J=6.9 Hz, 2H), 7.18 (t, J=7.5 Hz, 1H), 7.26 (d, J=8.2 Hz, 1H), 7.62 (t, J=7.2 Hz, 1H), 7.93 (d, J=8.0 Hz, 1H) 11.50 (s, 1H), 13.5 (s, 1H). EIMS m/z 234 (M+1), 256 (M+23). Anal. (C12H11NO4) C, H, N.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07514225B2uspto-grants-2009_04