تفاعل #1951070

ord-1a1aa3f008a145bbbffa7235814a5ff3

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe reaction mixture was concentrated by rotary evaporation
  2. 2
    استخلاصthe product was extracted into dichloromethane
  3. 3
    غسيلwashed with saturated brine
  4. 4
    تجفيفThe organic phase was dried with sodium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated by rotary evaporation
  7. 7
    أخرىto yield 2.52 g of crude product
  8. 8
    أخرىImpurities were removed
  9. 9
    غسيلThe product was then eluted from the silica with 10% methanol in ethyl acetate
  10. 10
    أخرىThe solvents were removed by rotary evaporation

الإجراء التجريبي

(4-Fluorophenyl) divinyl phosphine oxide (1.50 g, 7.65 mmol) and benzylamine (1.05 mL, 9.57 mmol) were dissolved in a mixture of 100 mL of THF and 100 mL of deionized water. The reaction mixture was heated at 90° C. overnight. The reaction mixture was concentrated by rotary evaporation and the product was extracted into dichloromethane and washed with saturated brine. The organic phase was dried with sodium sulfate, filtered, and concentrated by rotary evaporation to yield 2.52 g of crude product. Impurities were removed by passing a solution of the crude product in ethyl acetate through a plug of silica. The product was then eluted from the silica with 10% methanol in ethyl acetate. The solvents were removed by rotary evaporation to yield 1.89 g (6.24 mmol, 82%) of 1-benzyl-4-(4-fluorophenyl)-[1,4]azaphosphinane 4-oxide as a colorless oil. ESMS (m/z): (M+1)+ found, 304.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07625880B2uspto-grants-2009_12