Réaction #1929031

ord-c08a5405d5904f36a6efde542595a009

Équation de réaction

COB(OC)OC
trimethyl borate
c1ccc2c(c1)[se]c1ccccc12
dibenzoselenophene
Cl
HCl
[Li][CH2]CCC
BuLi
OB(O)c1cccc2c1[se]c1ccccc12
dibenzoselenophen-4-ylboronic acid

Solvants

Conditions de réaction

Température
-78°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction mixture was then heated
  2. 2
    Températureto reflux for 5 hours
  3. 3
    workup.WAITIt was then left
  4. 4
    ExtractionThe organic phase was extracted with ethyl acetate
  5. 5
    Séchagedried with sodium sulfate
  6. 6
    AutreThe combined organic phase was evaporated to dryness and 100 mL of 30% ethyl acetate in hexane
  7. 7
    workup.ADDITIONwas added to the solid
  8. 8
    workup.STIRRINGwith stirring at room temperature for 8 hours
  9. 9
    FiltrationThe suspension was filtered
  10. 10
    Lavagethe solids were washed with hexane
  11. 11
    Autredried
  12. 12
    Autreyielding 2 of white solids as the product which

Mode opératoire

4.0 g (17.3 mmol) of dibenzoselenophene and 150 mL of dry ether were added in a 250 mL three necked flask under nitrogen. To the mixture, 11.5 mL of BuLi (1.6 M in hexane) was added slowly at room temperature. The reaction mixture was then heated to reflux for 5 hours. The reaction mixture was cooled to −78° C. and 5 mL of trimethyl borate was added. It was then left to stir at room temperature for overnight. About 50 mL of 1 M HCl was added to the reaction mixture. The organic phase was extracted with ethyl acetate and dried with sodium sulfate. The combined organic phase was evaporated to dryness and 100 mL of 30% ethyl acetate in hexane was added to the solid with stirring at room temperature for 8 hours. The suspension was filtered, the solids were washed with hexane and dried, yielding 2 of white solids as the product which was confirmed by NMR

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08945727B2uspto-grants-2015_02