HRID1189604

反应详情

EQUATION

反应方程式

HRID 1189604 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Into a 200 mL three-neck flask were placed 0.90 g (5.7 mmol) of bromobenzene and 1.5 g (5.7 mol) of benzo[b]naphtho[1,2-d]furan-6-boronic acid, and the air in the flask was replaced with nitrogen. To this mixture were added 20 mL of toluene, 10 mL of ethanol, and 6.0 mL of an aqueous solution of sodium carbonate (2.0 mol/L). While the pressure was reduced, this mixture was stirred to be degassed. To this mixture was added 0.33 g (0.28 mmol) of tetrakis(triphenylphosphine)palladium(0), and the mixture was stirred at 80° C. for 2 hours under a nitrogen stream. After that, the aqueous layer of this mixture was subjected to extraction with toluene, and the obtained solution of the extract and the organic layer were combined and washed with saturated brine. The organic layer was dried with magnesium sulfate, and this mixture was gravity-filtered. An oily substance obtained by concentration of the obtained filtrate was purified by silica gel column chromatography (a developing solvent in which the ratio of hexane to toluene was 19:1) to give a white solid. The obtained solid was recrystallized with a mixed solvent of toluene and hexane, so that 0.95 g of white needle-like crystals of the object of the synthesis were obtained in 56% yield. The reaction scheme is illustrated in (R-1).

WORKUP

后处理

  1. customInto a 200 mL three-neck flask were placed
  2. customto be degassed
  3. stirringthe mixture was stirred at 80° C. for 2 hours under a nitrogen stream
  4. extractionAfter that, the aqueous layer of this mixture was subjected to extraction with toluene
  5. extractionthe obtained solution of the extract
  6. washwashed with saturated brine
  7. dry with materialThe organic layer was dried with magnesium sulfate
  8. filtrationthis mixture was gravity-filtered
  9. customAn oily substance obtained by concentration of the obtained filtrate
  10. customwas purified by silica gel column chromatography (a developing solvent in which the ratio of hexane to toluene
  11. customto give a white solid
  12. customThe obtained solid was recrystallized with a mixed solvent of toluene and hexane, so that 0.95 g of white needle-like crystals of the object of the synthesis
  13. customwere obtained in 56% yield
  14. customThe reaction scheme