Reacción #6684
ord-9c10f800168b48649bfb59f8e3d09d94
Ecuación de reacción
4-bromobutan-1-ol
3,4-dihydropyran
potassium carbonate
→
2-(4-bromobutoxy) -tetrahydropyran
2-(4-Bromobutoxy)tetrahydropyran
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.STIRRINGthe reaction mixture was stirred at room temperature for 1 h
- 2Otroquenched with water
- 3Extracciónextracted with dichloromethane
- 4Lavadowashed with brine
- 5Secadodried over MgSO4
- 6Concentraciónconcentrated in vacuo
- 7OtroPurification by chromatography on silica gel (5% EtOAc (ethylacetate)/hexanes)
Procedimiento
To a solution of commercially available 4-bromobutan-1-ol (16) (1 equi.) and 3,4-dihydropyran (17) (1.5 equi.) in dichloromethane (3 mL/mmole), phosphorus oxychloride (0.01 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h. Then potassium carbonate (1 equi.) was added to the reaction mixture and the reaction mixture was stirred at room temperature for 1 h, quenched with water, extracted with dichloromethane, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (5% EtOAc (ethylacetate)/hexanes) afforded 2-(4-bromobutoxy) -tetrahydropyran (18), as a colorless oil (88%).