反应 #84027

ord-aac163278d774f779aaceb5fc6c049d3

反应方程式

[H][H]
Hydrogen
[H][H]
Hydrogen
O=C(O)c1cccc([N+](=O)[O-])c1C(=O)O
3-nitrophthalic acid
[H][H]
hydrogen
Nc1cccc(C(=O)O)c1C(=O)O
3-aminophthalic acid
收率 84.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the mixture was purged with nitrogen 3 times
  2. 2
    过滤The suspension was filtered through a celite bed
  3. 3
    洗涤rinsed with methanol
  4. 4
    浓缩The filtrate was concentrated in vacuo
  5. 5
    其他isolated by vacuum filtration
  6. 6
    其他The solid was dried in vacuo to a constant weight

实验过程

10% Pd/C (2.5 g), 3-nitrophthalic acid (75.0 g, 355 mmol) and ethanol (1.5 L) were charged to a 2.5 L Parr hydrogenator under a nitrogen atmosphere. Hydrogen was charged to the reaction vessel for up to 55 psi. The mixture was shaken for 13 hours, maintaining hydrogen pressure between 50 and 55 psi. Hydrogen was released and the mixture was purged with nitrogen 3 times. The suspension was filtered through a celite bed and rinsed with methanol. The filtrate was concentrated in vacuo. The resulting solid was reslurried in ether and isolated by vacuum filtration. The solid was dried in vacuo to a constant weight, affording 54 g (84% yield) of 3-aminophthalic acid as a yellow product. 1H-NMR (DMSO-d6) δ: 3.17 (s, 2H), 6.67 (d, 1H), 6.82 (d, 1H), 7.17 (t, 1H), 8-10 (br, s, 2H); 13C-NMR (DMSO-d6) δ: 112.00, 115.32, 118.20, 131.28, 135.86, 148.82, 169.15, 170.09.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09433606B2uspto-grants-2016_09