تفاعل #215355

ord-f7c4956936af43d793c406cfa7a1a11f

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONA solution containing 30 g
  2. 2
    workup.DISTILLATIONThe ethanol and excess acetic anhydride is distilled off
  3. 3
    workup.ADDITIONthe residue is diluted with chloroform
  4. 4
    تركيزconcentrated
  5. 5
    درجة الحرارةcooled

الإجراء التجريبي

A solution containing 30 g. of benzoylacetonitrile, 36.4 g. of triethylorthopropionate and 57 g. of acetic anhydride is heated in an oil bath at 130° for 3 hours. The ethanol and excess acetic anhydride is distilled off and the residue is diluted with chloroform. The chloroform solution is passed quickly through Magnesol® and concentrated, then cooled to produce the title product. Similarly prepared is 2-benzoyl-3-methoxy-2-hexenonitrile and 2-benzoyl-3-methoxy-2-heptenonitrile.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04259256uspto-grants-1981_03