Réaction #2446097

ord-6c437c865f264842a4464ded9b704d09

Équation de réaction

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

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreequipped with a magnetic stirrer
  2. 2
    Autrethe internal temperature below 3° C
  3. 3
    workup.ADDITIONare added within 30 minutes
  4. 4
    TempératureAfter two hours the reaction mixture is warmed to room temperature
  5. 5
    Extractionextracted three times with 500 ml of Ethylacetate
  6. 6
    LavageThe 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
    Séchagedried over Magnesiumsulfate
  8. 8
    Filtrationfiltered
  9. 9
    Autreevaporated
  10. 10
    workup.DISSOLUTIONThe crude product is dissolved in Dichloromethane
  11. 11
    workup.ADDITION100 g of silica are added
  12. 12
    Autrethe 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
    Lavagethe product eluted with Hexane/Ethylacetate=8:1
  15. 15
    AutreThe product is crystallized from 2-Propanol

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08685541B2uspto-grants-2014_04