تفاعل #5609

ord-882500f88033402bbab10d05d86712f8

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe precipitate was collected by filtration
  2. 2
    غسيلwashed with ethyl acetate
  3. 3
    workup.DISSOLUTIONdissolved in dichloromethane (500 ml)
  4. 4
    workup.ADDITIONTo the solution were added water (300 ml) and 38% aqueous formaldehyde (100 ml)
  5. 5
    أخرىthe organic layer was separated
  6. 6
    غسيلwashed with water
  7. 7
    تجفيفdried over magnesium sulfate
  8. 8
    تركيزconcentrated under reduced pressure
  9. 9
    أخرىThe product was isolated by column chromatography on silica gel with ethyl acetate as an eluent

الإجراء التجريبي

A solution of 5-benzyloxy-2-chloromethyl-4-pyridone (10.0 g) and triphenylphosphine (10.5 g) in N,N-dimethylformamide (50 ml) was stirred for 5 hours at 90°-100° C. The resulting mixture was poured into ethyl acetate (800 ml). The precipitate was collected by filtration, washed with ethyl acetate and dissolved in dichloromethane (500 ml). To the solution were added water (300 ml) and 38% aqueous formaldehyde (100 ml). The mixture was adjusted to pH 10-10.5 with potassium carbonate. After being stirred for 3 hours at 35°-40° C., the organic layer was separated, washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The product was isolated by column chromatography on silica gel with ethyl acetate as an eluent to give 5-benzyloxy-2-vinyl-4-pyridone (6.02 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05244890uspto-grants-1993_09