反应 #2467933

ord-d1ff980968f943d1a2170927d015c4c1

反应方程式

O=Cc1cc(Br)cc(Br)c1
3,5-dibromobenzaldehyde
CC(C)(C)[O-].[K+]
potassium t-butoxide
[Cl-].[NH4+]
ammonium chloride
C=Cc1cc(Br)cc(Br)c1
3,5-dibromostyrene
收率 79.3%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cooling
  2. 2
    温度The resultant slurry was cooled to −78° C.
  3. 3
    workup.ADDITIONwas added dropwise
  4. 4
    温度to warm to room temperature
  5. 5
    workup.STIRRINGstirred for 1 hr
  6. 6
    萃取The product was extracted with ethyl acetate
  7. 7
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  8. 8
    其他the residue was purified with silica-gel column chromatography

实验过程

Tetrahydrofuran (20 mL) was added to methyltriphenylphosphonium bromide (3.150 g, 8.8 mmol). Then potassium t-butoxide (0.989 g, 8.8 mmol) was added herein small portions with ice-cooling, and the mixture was stirred at room temperature for 1 hr. The resultant slurry was cooled to −78° C. and a tetrahydrofuran (20 mL) solution containing 3,5-dibromobenzaldehyde (1.519 g, 5.8 mmol) was added dropwise. The reaction solution was allowed to warm to room temperature and stirred for 1 hr, and then a saturated ammonium chloride aqueous solution was added to the reaction solution. The product was extracted with ethyl acetate, the solvent was distilled off under reduced pressure, and the residue was purified with silica-gel column chromatography to obtain 3,5-dibromostyrene (1.2 g, 4.6 mmol).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08257837B2uspto-grants-2012_09