Реакция #1448

ord-d699a2fd0bfb49f2b2d9d51a6a3e6ab2

Уравнение реакции

N#CCc1ccccc1
benzyl cyanide
BrCCCCBr
1,4-dibromobutane
O
water
CCOC(C)=O
ethyl acetate
O=C(O)C1(c2ccccc2)CCCC1
1-phenylcyclopentanecarboxylic acid

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGagain stirred for 16 hours at room temperature
  2. 2
    Другоеthe resulting organic layer was separated
  3. 3
    Промывкаwashed with a saturated sodium chloride aqueous solution
  4. 4
    Сушкаdried over anhydrous magnesium sulfate
  5. 5
    ДругоеAfter removing the solvent
  6. 6
    workup.DISTILLATIONby distillation under a reduced pressure
  7. 7
    workup.ADDITIONthe resulting hexane eluate was mixed with 45 ml of sulfuric acid
  8. 8
    workup.WAITsubjected to 24 hours
  9. 9
    Температураof heating
  10. 10
    Температураunder reflux
  11. 11
    ТемператураAfter cooling down to room temperature
  12. 12
    workup.ADDITIONthe reaction solution was mixed with ice water and ethyl acetate
  13. 13
    Другоеto separate water layer which
  14. 14
    workup.ADDITIONwas subsequently mixed with concentrated hydrochloric acid and ethyl acetate
  15. 15
    Другоеthe resulting organic layer was separated
  16. 16
    Промывкаwashed with water
  17. 17
    Сушкаa saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate
  18. 18
    ДругоеBy removing the solvent
  19. 19
    workup.DISTILLATIONby distillation under a reduced pressure

Методика

In a stream of argon, 60% sodium hydride was dissolved in 10 ml of tetrahydrofuran, and the solution was mixed with 2.0 g of benzyl cyanide, stirred for 1 hour at room temperature, further mixed with 3.69 g of 1,4-dibromobutane and again stirred for 16 hours at room temperature. The reaction mixture was mixed with water and ethyl acetate, and the resulting organic layer was separated, washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. After removing the solvent by distillation under a reduced pressure, the thus obtained residue was subjected to silica gel column chromatography, and the resulting hexane eluate was mixed with 45 ml of sulfuric acid and subjected to 24 hours of heating under reflux. After cooling down to room temperature, the reaction solution was mixed with ice water and ethyl acetate to separate water layer which was subsequently mixed with concentrated hydrochloric acid and ethyl acetate, and the resulting organic layer was separated, washed with water and a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. By removing the solvent by distillation under a reduced pressure, 978 mg of 1-phenylcyclopentanecarboxylic acid was obtained.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723606uspto-grants-1998_03