Reacción #6684

ord-9c10f800168b48649bfb59f8e3d09d94

Ecuación de reacción

OCCCCBr
4-bromobutan-1-ol
C1=COCCC1
3,4-dihydropyran
O=C([O-])[O-].[K+].[K+]
potassium carbonate
BrCCCCOC1CCCCO1
2-(4-bromobutoxy) -tetrahydropyran
BrCCCCOC1CCCCO1
2-(4-Bromobutoxy)tetrahydropyran

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe reaction mixture was stirred at room temperature for 1 h
  2. 2
    Otroquenched with water
  3. 3
    Extracciónextracted with dichloromethane
  4. 4
    Lavadowashed with brine
  5. 5
    Secadodried over MgSO4
  6. 6
    Concentraciónconcentrated in vacuo
  7. 7
    OtroPurification 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%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07083832B2uspto-grants-2006_08