反应 #6684
ord-9c10f800168b48649bfb59f8e3d09d94
反应方程式
4-bromobutan-1-ol
3,4-dihydropyran
potassium carbonate
→
2-(4-bromobutoxy) -tetrahydropyran
2-(4-Bromobutoxy)tetrahydropyran
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1workup.STIRRINGthe reaction mixture was stirred at room temperature for 1 h
- 2其他quenched with water
- 3萃取extracted with dichloromethane
- 4洗涤washed with brine
- 5干燥dried over MgSO4
- 6浓缩concentrated in vacuo
- 7其他Purification by chromatography on silica gel (5% EtOAc (ethylacetate)/hexanes)
实验过程
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%).