反応 #2467964

ord-6840d895f9b141e48b3313a57056022e

反応方程式

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
収率 91.0%
COC(=O)c1sccc1N=NN(C)C
Methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate
収率 91.0%

溶媒

反応条件

温度
2.5°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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.

出典

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