تفاعل #95251

ord-4f2359555168413fb3d83b5c45b8f9c5

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto maintain
  2. 2
    workup.DISTILLATIONa steady distillation of acetic acid
  3. 3
    أخرىfrom the reaction through a helix-packed fractionation column
  4. 4
    درجة الحرارةto maintain a constant volume until complete conversion of starting materials to product
  5. 5
    درجة الحرارةThe mixture is cooled
  6. 6
    أخرىpartitioned between 2 l
  7. 7
    درجة الحرارةof cold water containing solid sodium bicarbonate to maintain a neutral pH
  8. 8
    غسيلThe organic phase is washed with saturated brine
  9. 9
    تجفيفdried (MgSO4)
  10. 10
    أخرىevaporated
  11. 11
    أخرىto yield 452 g

الإجراء التجريبي

A solution of 400 g. (2.04 moles) of a mixture of 2-(5-hydroxypentyl)cyclopentanone and 2-(5-acetoxypentyl)cyclopentanone (Example 55) and 4.0 g. of p-toluenesulfonic acid monohydrate in 1 l. of acetic anhydride is refluxed at a rate to maintain a steady distillation of acetic acid from the reaction through a helix-packed fractionation column. The reaction is continued with the addition of acetic anhydride to maintain a constant volume until complete conversion of starting materials to product is evident. The mixture is cooled and partitioned between 2 l. of hexane and 3 l. of cold water containing solid sodium bicarbonate to maintain a neutral pH. The organic phase is washed with saturated brine. dried (MgSO4), and evaporated to yield 452 g. of an oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04343949uspto-grants-1982_08