تفاعل #1583875

ord-46599b8306124f56911108474c6cb3f3

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTo a 10 L reaction flask
  2. 2
    أخرىAfter the completion of reaction
  3. 3
    أخرىthe reaction solution was evaporated under reduced pressure
  4. 4
    أخرىto remove acetonitrile
  5. 5
    workup.ADDITIONA mixed solution of dichloromethane and water was added for extraction
  6. 6
    تجفيفThe organic phase was dried over anhydrous sodium sulfate
  7. 7
    أخرىevaporated
  8. 8
    أخرىto remove the solvent
  9. 9
    أخرىto produce a crude product, which
  10. 10
    أخرىwas purified by column chromatography (silica gel column, eluted with petroleum ether: ethyl acetate=50:1 (volumetric ratio))

الإجراء التجريبي

To a 10 L reaction flask were added 3-methylpyrrolidin-3-ol hydrochloride (616 g, 4.48 mol), anhydrous potassium carbonate (1186 g, 8.6 mol) and acetonitrile (5 L). To the resulting mixture was slowly added a solution of 3,3-diphenylpropyl methanesulfonate (1000 g, 3.45 mol) in acetonitrile dropwisely at 85° C. The reaction was conducted for 12 hours. After the completion of reaction monitored by TLC, the reaction solution was evaporated under reduced pressure to remove acetonitrile. A mixed solution of dichloromethane and water was added for extraction. The organic phase was dried over anhydrous sodium sulfate, and evaporated to remove the solvent to produce a crude product, which was purified by column chromatography (silica gel column, eluted with petroleum ether: ethyl acetate=50:1 (volumetric ratio)) to produce 1-(3,3-diphenylpropyl)-3-methylpyrrolidin-3-ol (580 g) in a yield of 57%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09198902B2uspto-grants-2015_12