Reaction #6684

ord-9c10f800168b48649bfb59f8e3d09d94

Reaction equation

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

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.STIRRINGthe reaction mixture was stirred at room temperature for 1 h
  2. 2
    Otherquenched with water
  3. 3
    Extractionextracted with dichloromethane
  4. 4
    Washwashed with brine
  5. 5
    Dryingdried over MgSO4
  6. 6
    Concentrationconcentrated in vacuo
  7. 7
    OtherPurification by chromatography on silica gel (5% EtOAc (ethylacetate)/hexanes)

Procedure

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%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07083832B2uspto-grants-2006_08