تفاعل #998769

ord-e83e432ffaa347be8dc384504ae70d63

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةHeat the mixture
  2. 2
    درجة الحرارةto reflux overnight
  3. 3
    تركيزconcentrate in vacuo
  4. 4
    أخرىPartition the residue between EtOAc and 5N aqueous HCl
  5. 5
    غسيلwash the acidic aqueous phase again with 5N aqueous HCl
  6. 6
    استخلاصExtract the basic aqueous solution three times with chloroform
  7. 7
    تجفيفDry the combined organic extracts over Na2SO4
  8. 8
    ترشيحfilter
  9. 9
    تركيزconcentrate in vacuo

الإجراء التجريبي

Add hydrazine hydrate (0.189 mL, 3.913 mmol) to a stirred suspension of 2-[4-(3,3-dimethyl-butyryl)-benzyl]-isoindole-1,3-dione (875 mg, 2.609 mmol) in methanol (15 mL). Heat the mixture to reflux overnight. Cool the mixture to room temperature and concentrate in vacuo. Partition the residue between EtOAc and 5N aqueous HCl and wash the acidic aqueous phase again with 5N aqueous HCl. Basify with 5N aqueous NaOH to pH 12. Extract the basic aqueous solution three times with chloroform. Dry the combined organic extracts over Na2SO4, filter and concentrate in vacuo to give the title compound as a yellow oil (411 mg, 77%) that was used without any further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08022062B2uspto-grants-2011_09