تفاعل #63801

ord-eaa8136f564341ca92b105370cbd5130

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىanhydrous oxygen gas was rapidly bubbled through the resulting solution
  2. 2
    workup.STIRRINGto stir for an additional hour
  3. 3
    أخرىOxygenation
  4. 4
    أخرىthe reaction was quenched by the addition of 50 ml of acetic acid
  5. 5
    تركيزThe reaction mixture was then concentrated
  6. 6
    workup.DISSOLUTIONthe residue dissolved in ethyl acetate
  7. 7
    غسيلThe organic solution was washed successively with 1N hydrochloric acid, saturated sodium bicarbonate, and brine
  8. 8
    تجفيفdried over anhydrous sodium sulfate
  9. 9
    أخرىConcentration of the dried organic solution afforded a solid which

الإجراء التجريبي

A solution of 7-chloro-1,3,4,5-tetrahydro-3-(methoxycarbonyl)-4-(4-methoxyphenyl)-2H-1-benzazepin-2-one (15 g, 41.7 mmole) in 780 ml of tetrahydrofuran was cooled to -78° C. and 147 ml (167 mmole in tetrahydrofuran) of potassium hexamethyldisilazide solution was added. After stirring for 1 hour, 28.7 ml of triethyl phosphite (166.7 mmole) was added and anhydrous oxygen gas was rapidly bubbled through the resulting solution. The reaction temperature was then raised to 0° C. and allowed to stir for an additional hour. Oxygenation was then discontinued and the reaction was quenched by the addition of 50 ml of acetic acid. The reaction mixture was then concentrated and the residue dissolved in ethyl acetate. The organic solution was washed successively with 1N hydrochloric acid, saturated sodium bicarbonate, and brine and then dried over anhydrous sodium sulfate. Concentration of the dried organic solution afforded a solid which, upon trituration in hexane, gave 14.8 g of the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04767756uspto-grants-1988_08