Reacción #67962
ord-1a20acba42b44c2fb88c7da546c2a2e8
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otrothe solvent was removed under reduced pressure
- 2OtroThe residue thus obtained
- 3OtroThe aqueous layer was separated
- 4workup.ADDITIONethyl acetate was added
- 5OtroThe organic layer was separated
- 6Secadodried over potassium carbonate
- 7Otrothe solvent was removed under reduced pressure
Procedimiento
To 0.60 g of 1-tert-butyl 3-ethyl 4-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)piperazine-1,3-dicarboxylate, 12 mL of 10 mol/L hydrogen chloride/ethanol was added, and the mixture was stirred for 2 hours, and then the solvent was removed under reduced pressure. The residue thus obtained was added with water and ethyl acetate. The aqueous layer was separated, ethyl acetate was added thereto, and the resultant solution was adjusted to pH 14 with a 5 mol/L aqueous sodium hydroxide solution. The organic layer was separated and dried over potassium carbonate, and the solvent was removed under reduced pressure to obtain 0.34 g of a brown oily substance, ethyl 1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)piperazine-2-carboxylate.