反应 #927255

ord-563397aa91c04bb2a6ddbf7fb67ad896

反应方程式

CCCCCC
hexane
[Na+].[OH-]
sodium hydroxide
CCCCCCO
hexanol
C=C(Br)CBr
2,3-dibromopropene
C=C(Br)COCCCCCC
2-bromo-3-hexyloxypropene
收率 95.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他To a three neck round bottom flask equipped with an addition funnel and an overhead stirrer
  2. 2
    其他were fed to the well-stirred reaction mixture over a 20 minute period
  3. 3
    其他the phases were separated
  4. 4
    洗涤The organic phase was washed with water and brine
  5. 5
    干燥dried over magnesium sulfate
  6. 6
    过滤filtered
  7. 7
    workup.DISTILLATIONThe product was fractionally distilled under reduced pressure

实验过程

To a three neck round bottom flask equipped with an addition funnel and an overhead stirrer was added 35 ml of hexane, 42 g of 50% sodium hydroxide and 0.50 g of tetra-n-butylammonium bromide. A mixture of 6.74 g of hexanol (66 mmol) and 20 g (100 mmol) of 2,3-dibromopropene were fed to the well-stirred reaction mixture over a 20 minute period. The reaction was stirred an additional 1 hour, then water was added, and the phases were separated. The organic phase was washed with water and brine, dried over magnesium sulfate, filtered and stripped. The product was fractionally distilled under reduced pressure to give 6.1 g of 95% pure 2-bromo-3-hexyloxypropene.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06365549B2uspto-grants-2002_04