Reacción #50422
ord-0b48dd619f2a4b93b2a672614333945e
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.DISSOLUTIONto dissolve the solid
- 2workup.STIRRINGwas stirred at room temperature for 20 hours after which it
- 3ExtracciónThe mixture was then extracted with methylene chloride
- 4SecadoThe extract was dried over sodium sulfate
- 5Otroevaporated
- 6workup.DISSOLUTIONThe residue was dissolved in 100 of toluene, and 100 mg of p-toluenesulfonic acid
- 7workup.ADDITIONwas added
- 8TemperaturaThe mixture then was refluxed for 1.5 hours after which it
- 9workup.ADDITIONwas poured into water
- 10Extracciónextracted with methylene chloride
- 11ExtracciónThe methylene chloride extract
- 12Secadowas dried over sodium sulfate
- 13Otroevaporated
Procedimiento
Potassium t-butoxide (0.82 g; 7.3 mmol) was suspended in 100 ml of tetrahydrofuran (THF). Ethyl formate (1.0 g; 13.3 mmol) and 2-di-n-propylamino-8-butyryl-1,2,3,4-tetrahydronaphthalene (1.0 g; 3.3 mmol) in THF was added to the mixture. The resulting mixture was stirred at room temperature overnight. Hydroxylamine (1.2 g; 16.6 mmol) was added followed by sufficient water to dissolve the solid. The resulting mixture, having pH 6, was stirred at room temperature for 20 hours after which it was poured into water, and the pH was adjusted to 12 with ammonium hydroxide. The mixture was then extracted with methylene chloride. The extract was dried over sodium sulfate and evaporated. The residue was dissolved in 100 of toluene, and 100 mg of p-toluenesulfonic acid was added. The mixture then was refluxed for 1.5 hours after which it was poured into water and extracted with methylene chloride. The methylene chloride extract was dried over sodium sulfate and evaporated.