反应 #2467965

ord-6fca64d3a1884b18955fbf65c9878219

反应方程式

[NH4+].[OH-]
ammonium hydroxide
COC(=O)c1sccc1N=NN(C)C
Methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate
O=S(=O)(O)O
sulfuric acid
O=[N+]([O-])O
nitric acid
COC(=O)c1sc([N+](=O)[O-])cc1N=NN(C)C
solid
收率 26.0%
COC(=O)c1sc([N+](=O)[O-])cc1N=NN(C)C
Methyl 3-[(dimethylamino)diazenyl]-5-nitrothiophene-2-carboxylate
收率 26.0%

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The solution was extracted with chloroform (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 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate (2 g, 9.38 mmol) was added slowly for 15 min at 0 to −5° C. to concentrated sulfuric acid (20 mL). Then concentrated nitric acid (0.54 mL, 70%, 10.7 mmol) was added to the above reaction mixture for 10 min and stirred at the same temperature for 1 h and rt for 16 h. The mixture was poured into ice cooled water and basified with ammonium hydroxide. The solution was extracted with chloroform (3×100 mL) and 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 hexane-ethyl acetate (80:20) as eluents to give the product as a yellow color solid (450 mg, 26%), mp 128-130° C.

来源

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