تفاعل #54346

ord-8b69a75568a74b1c9e91c4639bbb9fe6

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTo a 0° C.
  2. 2
    workup.ADDITIONis then added to 250 ml
  3. 3
    تجفيفThe ether phase is dried over magnesium sulfate
  4. 4
    أخرىevaporated
  5. 5
    أخرىThe residue is purified via column chromatography on 200 g
  6. 6
    غسيلof silica gel eluted with 50% ether-cyclohexane

الإجراء التجريبي

To a 0° C. solution of 7.0 mmols. of 3-phenylpropylmagnesium bromide in 7 ml. of tetrahydrofuran is slowly added a solution of 2.48 g. (5.0 mmols.) of 1-benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidone in 10 ml. of tetrahydrofuran. The resultant mixture is stirred for one hour and is then added to 250 ml. of saturated ammonium chloride-250 ml. ether. The ether phase is dried over magnesium sulfate and evaporated. The residue is purified via column chromatography on 200 g. of silica gel eluted with 50% ether-cyclohexane to yield the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04147872uspto-grants-1979_04