تفاعل #47815

ord-93b0980d393d482f97ea807b4febef77

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىUpon the completion of the reaction
  2. 2
    غسيلthe mixture washed with saturated saline
  3. 3
    استخلاصextracted with dichloromethane
  4. 4
    أخرىThe organic layer was separated
  5. 5
    تجفيفdried over anhydrous MgSO4
  6. 6
    تركيزconcentrated under a reduced pressure
  7. 7
    أخرىThe resulting residue was purified by flash chromatography (ethyl acetate:hexane=1:5)

الإجراء التجريبي

3-Phenyl-6-(3-phenyl-propoxy)-indene-1-one (200 mg, 0.586 mmol) obtained in Step 1 was dissolved in carbon tetrachloride, and N-bromosuccinimide (313 mg, 1.75 mmol) and 2,2′-azobisisobutyronitrile (9.7 mg) were added thereto. The mixture was refluxed for 1 hr under the irradiation of a 375 W tungsten lamp. Upon the completion of the reaction, the mixture washed with saturated saline and extracted with dichloromethane. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography (ethyl acetate:hexane=1:5) to obtain 147 mg of the titled compound (yield: 60%) as a red solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745439B2uspto-grants-2010_06