반응 #94169

ord-2c38ccc94d1546ba92a2bed4bc5bdd04

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONround bottom flask containing a thermometer, condenser and magnetic stirring bar
  2. 2
    workup.ADDITIONwas added 4.0 g
  3. 3
    기타did not rise above 25° C
  4. 4
    workup.ADDITIONAfter completion of the addition the reaction mixture
  5. 5
    workup.ADDITIONdiluted with 100 ml
  6. 6
    기타The ether layer was separated
  7. 7
    세척washed consecutively with 5% HCl, water, and 10% NaHCO3 solution and saturated sodium chloride solution
  8. 8
    기타The ether was evaporated off
  9. 9
    workup.DISSOLUTIONthe residue dissolved in methylene chloride
  10. 10
    건조dried over anhydrous sodium sulfate
  11. 11
    여과filtered

실험 절차

To a solution of 4.7 g. (0.022 m) of 2,4-dihydroxybenzophenone and 2.5 ml. of pyridine in 35 ml. of ether in a 4 neck 100 ml. round bottom flask containing a thermometer, condenser and magnetic stirring bar was added 4.0 g. (0.0218 m) of 4-t-butylazo-4-cyanovaleryl chloride dropwise with cooling so the temperature did not rise above 25° C. After completion of the addition the reaction mixture was stirred 1/2 hour at room temperature and then diluted with 100 ml. of water. The ether layer was separated, washed consecutively with 5% HCl, water, and 10% NaHCO3 solution and saturated sodium chloride solution. The ether was evaporated off and the residue dissolved in methylene chloride, dried over anhydrous sodium sulfate, filtered and the methylene chloride stripped off under reduced pressure. The product weighted 8.8 g. (99% yield) and was a viscous syrup. The infrared spectrum was in agreement with the structure of the desired product.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04129586uspto-grants-1978_12