Reacción #2467974
ord-32927d07dc9a4b12b90a4504c6ae7db0
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONThe mixture was diluted with ice cold water
- 2Extracciónextracted with chloroform
- 3LavadoThe combined chloroform layer was washed with water, brine
- 4Secadodried over sodium sulfate
- 5FiltraciónThe solution was filtered
- 6Otroevaporated the solvent
- 7OtroThe residue was chromatographed over silica gel column
Procedimiento
To a solution of methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate (200 mg, 0.93 mmol) in methanol (10 mL) was added a solution of sodium hydroxide (93 mg, 2.3 mmol) in water (2 mL) and stirred at rt for 2 h. The mixture was diluted with ice cold water and acidified with dil. HCl and extracted with chloroform. The combined chloroform 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 an off-white solid (70 mg, 38%), mp 108-110° C. IR (neat) νmax 3402, 3082, 2923, 1708, 1218, 1116, 1066, 1016, 880, 773 cm−1; 1H NMR (400 MHz, CDCl3): δ 12.21 (1H, s), 7.47 (1H, d, J=5.2 Hz), 7.30 (1H, d, J=5.2 Hz), 3.65 (3H, s), 3.28 (3H, s); LC-MS (positive ion mode): m/z 200 (M+H)+.