تفاعل #998769
ord-e83e432ffaa347be8dc384504ae70d63
معادلة التفاعل
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةHeat the mixture
- 2درجة الحرارةto reflux overnight
- 3تركيزconcentrate in vacuo
- 4أخرىPartition the residue between EtOAc and 5N aqueous HCl
- 5غسيلwash the acidic aqueous phase again with 5N aqueous HCl
- 6استخلاصExtract the basic aqueous solution three times with chloroform
- 7تجفيفDry the combined organic extracts over Na2SO4
- 8ترشيحfilter
- 9تركيزconcentrate 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.