反应 #2467964

ord-6840d895f9b141e48b3313a57056022e

反应方程式

O=C([O-])[O-].[K+].[K+]
K2CO3
CNC
dimethylamine
COC(=O)c1sccc1N
methyl 3-aminothiophene-2-carboxylate
Cl
HCl
O=N[O-].[Na+]
NaNO2
COC(=O)c1sccc1N=NN(C)C
solid
收率 91.0%
COC(=O)c1sccc1N=NN(C)C
Methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate
收率 91.0%

溶剂

反应条件

温度
2.5°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGThe mixture was stirred at 0-10° C. for 1 h
  2. 2
    workup.ADDITIONpoured into ice cold water
  3. 3
    萃取The solution was extracted with chloroform (3×100 mL)
  4. 4
    洗涤The combined layer was washed with water, brine
  5. 5
    干燥dried over sodium sulfate
  6. 6
    过滤The solution was filtered
  7. 7
    其他evaporated the solvent
  8. 8
    其他The residue was chromatographed over silica gel column

实验过程

To a solution of methyl 3-aminothiophene-2-carboxylate (2.0 g, 12.7 mmol) and conc. HCl (5 mL, 50.8 mmol) in H2O (30 mL) was added NaNO2 (0.96 g, 14.08 mmol) in portions for 5 min at 0° C. After stirring 0.5 h (0-5° C.), the reaction mixture was added to the solution of K2CO3 (6.65 g, 48.26 mmol) and dimethylamine (5.14 mL, 40%, 45.7 mmol) in H2O (36 mL) at 0° C. The mixture was stirred at 0-10° C. for 1 h and poured into ice cold water. The solution was extracted with chloroform (3×100 mL). The combined 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-EtOAc (80:20) as eluents to give the product as a pale orange color solid (2.5 mg, 91%), mp 74-76° C.

来源

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