تفاعل #4100

ord-0d50972b8c6f417dabdfd558c12a27e4

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe catalyst was then removed by filtration
  2. 2
    تركيزthe filtrate was concentrated in vacuo to an oil
  3. 3
    workup.DISSOLUTIONThis was dissolved in 30 ml of ethanol
  4. 4
    workup.ADDITION30 ml of ether saturated with hydrogen chloride was added
  5. 5
    workup.ADDITIONAn additional 500 ml of plain ether was added
  6. 6
    workup.STIRRINGthe mixture was stirred at 0° C.
  7. 7
    أخرىprecipitation
  8. 8
    أخرىThe hydrochloride salt was collected
  9. 9
    أخرىdried
  10. 10
    أخرىRecrystallization from ethanol (charcoal)

الإجراء التجريبي

A Parr bottle, charged with 12.4 g (0.040 mole) of 5-chloro-1-(4-chloro-2-nitrophenyl)indoline of Example 8a, 100 ml of benzene, 100 ml of absolute ethanol and 0.5 g of 1% Pt/C was shaken under an initial hydrogen pressure of 57 psig until uptake ceased. The catalyst was then removed by filtration and the filtrate was concentrated in vacuo to an oil weighing 11.2 g (100%). This was dissolved in 30 ml of ethanol and then 30 ml of ether saturated with hydrogen chloride was added. An additional 500 ml of plain ether was added, and the mixture was stirred at 0° C., to maximize precipitation. The hydrochloride salt was collected, dried, and found to weigh 9.2 g (73%), m.p. 174°-178° C. Recrystallization from ethanol (charcoal) afforded 1-(2-amino-4-chlorophenyl)-5-chloroindoline hydrochloride ethanolate in 58% overall yield, m.p. 177°-180° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04723007uspto-grants-1988_02