Reacción #2467964
ord-6840d895f9b141e48b3313a57056022e
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.STIRRINGThe mixture was stirred at 0-10° C. for 1 h
- 2workup.ADDITIONpoured into ice cold water
- 3ExtracciónThe solution was extracted with chloroform (3×100 mL)
- 4LavadoThe combined layer was washed with water, brine
- 5Secadodried over sodium sulfate
- 6FiltraciónThe solution was filtered
- 7Otroevaporated the solvent
- 8OtroThe residue was chromatographed over silica gel column
Procedimiento
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.