تفاعل #63259

ord-d54822879ad64c44a320d371522417f1

ظروف التفاعل

درجة الحرارة
-15°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرى3-neck round bottom flask was purged with nitrogen
  2. 2
    درجة الحرارةwhile maintaining the temperature of the reaction mixture between about -15° C. and about -17° C
  3. 3
    أخرىThe stirred reaction mixture
  4. 4
    درجة الحرارةto warm to room temperature
  5. 5
    workup.STIRRINGthe mixture was stirred for 1 hour
  6. 6
    درجة الحرارةThe reaction mixture was cooled to about -25° C.
  7. 7
    workup.STIRRINGThe resulting mixture was stirred for about 30 minutes at about -25° C.
  8. 8
    درجة الحرارةto warm to about 5° C
  9. 9
    درجة الحرارةThe mixture was cooled to about -15° C.
  10. 10
    درجة الحرارةThe mixture was warmed to about 0° C.
  11. 11
    أخرىThe stirred reaction mixture
  12. 12
    درجة الحرارةwas cooled to about -37° C
  13. 13
    درجة الحرارةThe reaction mixture was warmed to about 0° C. over a period of about 65 minutes
  14. 14
    workup.WAITthe mixture was held at this temperature for 17.5 hours

الإجراء التجريبي

A 1 l. 3-neck round bottom flask was purged with nitrogen and charged with 35.0 g (0.312 mol) of potassium t-butoxide. Next, 348 ml of dry tetrahydrofuran was added to the flask and the resulting mixture was cooled to about -15° C. with stirring. To this mixture was added a solution of 30.3 g (0.155 mol) of (8aR-trans)-(-)-octahydro-1-(n-propyl)-6-(2H)-quinolinone in 30 ml of tetrahydrofuran over a period of about 9 minutes while maintaining the temperature of the reaction mixture between about -15° C. and about -17° C. The stirred reaction mixture was allowed to warm to room temperature and the mixture was stirred for 1 hour. The reaction mixture was cooled to about -25° C. and a solution of 23.1 g (25.2 ml, 0.31 mol) of ethyl formate in 45 ml of tetrahydrofuran was added dropwise to the reaction mixture over a period of about 21 minutes. The resulting mixture was stirred for about 30 minutes at about -25° C. and was allowed to warm to about 5° C. The mixture was cooled to about -15° C. and held at that temperature for about 60 hours. The mixture was warmed to about 0° C. and charged with 8.9 ml of glacial acetic acid dropwise. The stirred reaction mixture was cooled to about -37° C. To the mixture was added a solution of 32.6 g (0.171 mol) of p-toluenesulfonyl chloride dissolved in 45 ml of tetrahydrofuran over a period of about 5 minutes. The reaction mixture was warmed to about 0° C. over a period of about 65 minutes and the mixture was held at this temperature for 17.5 hours. The title compound thus prepared was held in situ for further processing.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04764609uspto-grants-1988_08