تفاعل #347685

ord-5e6e85e2d9d8426d99779a089a22f9f3

الكواشف

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المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزAt the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure
  2. 2
    workup.ADDITIONpoured into water
  3. 3
    استخلاصextracted with diethyl ether
  4. 4
    غسيلThe extract was washed with 5% w/v aqueous hydrochloric acid, with a 5% w/v aqueous solution of sodium bicarbonate and with water, in that order
  5. 5
    تجفيفdried over anhydrous magnesium sulfate
  6. 6
    أخرىThe solvent was then removed by distillation under reduced pressure
  7. 7
    أخرىto give a crude product
  8. 8
    أخرىThis was purified by column chromatography through silica gel
  9. 9
    غسيلeluted with a 2:1 by volume mixture of cyclohexane and ethyl acetate

الإجراء التجريبي

2(b) 314 μl of 1,8-diaza[5.4.0]-7-undecene were added to a solution of 620 mg of diethyl 2-(3-bromopropionamido)malonate (prepared as described above) dissolved in methylene chloride, and the mixture was stirred at room temperature for 3 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure, poured into water and then extracted with diethyl ether. The extract was washed with 5% w/v aqueous hydrochloric acid, with a 5% w/v aqueous solution of sodium bicarbonate and with water, in that order, and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, to give a crude product. This was purified by column chromatography through silica gel, eluted with a 2:1 by volume mixture of cyclohexane and ethyl acetate, to give 171 mg of diethyl 2-oxopyrrolidine-5,5-dicarboxylate.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05527905uspto-grants-1996_06