تفاعل #741806

ord-cdd6ab6518924715a1a2b66a513c6179

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added slowly
  2. 2
    درجة الحرارةThe mixture was refluxed for 3 hours
  3. 3
    أخرىEtOH was removed under vacuum
  4. 4
    ترشيحThe solid was filtered
  5. 5
    غسيلwashed with toluene (3×) and ether (3×)
  6. 6
    workup.DISSOLUTIONThe solid dissolved
  7. 7
    أخرىa brown oil formed
  8. 8
    استخلاصThe oil was extracted with ether (3×)
  9. 9
    غسيلthe combined ether extracts were washed with H2O (2×), saturated NaCl (2×)
  10. 10
    تجفيفwas finally dried over MgSO4
  11. 11
    أخرىThe ether was removed under vacuum

الإجراء التجريبي

1.4 g of sodium was dissolved in absolute EtoH with warming to 70° C., then EtOH was removed under vacuum to give a white solid residue of NaOEt. A mixture of 35 ml of diethyl carbonate, 43 ml of toluene, 13.46 g of 3-methoxy-5-methylthio-4-propoxyphenyl acetonitrile was added slowly. The mixture was refluxed for 3 hours. EtOH was removed under vacuum. The solid was filtered and washed with toluene (3×) and ether (3×). The solid was suspended in 200 ml of H2O and acidified with 6N HCl. The solid dissolved and a brown oil formed. The oil was extracted with ether (3×), the combined ether extracts were washed with H2O (2×), saturated NaCl (2×) was finally dried over MgSO4. The ether was removed under vacuum to give 16 g (92% yield) of ethyl 3-methoxy-5-methylthio-4-propoxy-α-cyanobenzeneacetate.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05132463uspto-grants-1992_07