Reacción #2446097

ord-6c437c865f264842a4464ded9b704d09

Ecuación de reacción

O
water
O=Cc1ccc2oc3ccccc3c2c1
Dibenzofuran-2-carboxaldehyde
[Li][CH2]CCC
Butyl lithium
C=Cc1ccc2oc3ccccc3c2c1
2-Vinyl-dibenzofuran
Rendimiento 95.0%

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroequipped with a magnetic stirrer
  2. 2
    Otrothe internal temperature below 3° C
  3. 3
    workup.ADDITIONare added within 30 minutes
  4. 4
    TemperaturaAfter two hours the reaction mixture is warmed to room temperature
  5. 5
    Extracciónextracted three times with 500 ml of Ethylacetate
  6. 6
    LavadoThe combined organic phases are washed once with 500 ml of a 1:1 mixture of buffer pH=1 and brine, once with 30 ml of brine
  7. 7
    Secadodried over Magnesiumsulfate
  8. 8
    Filtraciónfiltered
  9. 9
    Otroevaporated
  10. 10
    workup.DISSOLUTIONThe crude product is dissolved in Dichloromethane
  11. 11
    workup.ADDITION100 g of silica are added
  12. 12
    Otrothe solvent is evaporated
  13. 13
    workup.ADDITIONThe resulting powder is added on top of 300 g of silica in a sintered glass funnel
  14. 14
    Lavadothe product eluted with Hexane/Ethylacetate=8:1
  15. 15
    OtroThe product is crystallized from 2-Propanol

Procedimiento

22.7 g (63.7 mmol) of Methyl triphenylphosphonium bromide and 200 ml of dry THF are placed in a dried 500 ml three necked round bottomed flask, equipped with a magnetic stirrer and the reaction mixture is cooled to 0° C. internal temperature with a NaCl/ice bath. 41.8 ml (66.9 mmol) of 1.6 M Butyl lithium solution in Hexane are added within 30 minutes while keeping the internal temperature below 3° C. The reaction mixture is stirred at the same temperature for 45 minutes, then 47.2 mmol of Dibenzofuran-2-carboxaldehyde dissolved in 100 ml of dry THF are added within 30 minutes. After two hours the reaction mixture is warmed to room temperature, added to 500 ml of water and extracted three times with 500 ml of Ethylacetate. The combined organic phases are washed once with 500 ml of a 1:1 mixture of buffer pH=1 and brine, once with 30 ml of brine, dried over Magnesiumsulfate, filtered and evaporated. The crude product is dissolved in Dichloromethane, 100 g of silica are added and the solvent is evaporated. The resulting powder is added on top of 300 g of silica in a sintered glass funnel and the product eluted with Hexane/Ethylacetate=8:1. The product is crystallized from 2-Propanol. 2-Vinyl-dibenzofuran is isolated in 95% yield.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08685541B2uspto-grants-2014_04