反应 #2467967

ord-2ed853de447e46498067723a1a038e31

反应方程式

COC(=O)c1cc(O)c(C(=O)OC)s1
Methyl 4-hydroxy-5-(methoxycarbonyl)thiophene-2-carboxylate
O=S(=O)(O)O
sulfuric acid
O=[N+]([O-])O
nitric acid
COC(=O)c1sc(C(=O)OC)c([N+](=O)[O-])c1O
semi-solid
收率 20.0%
COC(=O)c1sc(C(=O)OC)c([N+](=O)[O-])c1O
Methyl 4-hydroxy-5-(methoxycarbonyl)-3-nitrothiophene-2-carboxylate
收率 20.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONThe mixture was poured into ice
  2. 2
    萃取extracted with ethyl acetate (3×100 mL)
  3. 3
    洗涤The combined organic layer was washed with water, brine
  4. 4
    干燥dried over sodium sulfate
  5. 5
    过滤The solution was filtered
  6. 6
    其他evaporated the solvent
  7. 7
    其他The residue was chromatographed over silica gel column

实验过程

Methyl 4-hydroxy-5-(methoxycarbonyl)thiophene-2-carboxylate (5 g, 23.14 mmol) was added slowly for 15 min at 0 to −5° C. to concentrated sulfuric acid (25 mL). Then concentrated nitric acid (3.2 mL, 70%, 34.7 mmol) was added to the above reaction mixture for 10 min and stirred at the same temperature for 1 h. The mixture was poured into ice cooled water and extracted with ethyl acetate (3×100 mL). The combined organic layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using chloroform-methanol (95:5) as eluents to give the product as a yellow color semi-solid (1.2 g, 20%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08258119B2uspto-grants-2012_09