تفاعل #1951070
ord-1a1aa3f008a145bbbffa7235814a5ff3
معادلة التفاعل
الكواشف
ظروف التفاعل
المعالجة
- 1تركيزThe reaction mixture was concentrated by rotary evaporation
- 2استخلاصthe product was extracted into dichloromethane
- 3غسيلwashed with saturated brine
- 4تجفيفThe organic phase was dried with sodium sulfate
- 5ترشيحfiltered
- 6تركيزconcentrated by rotary evaporation
- 7أخرىto yield 2.52 g of crude product
- 8أخرىImpurities were removed
- 9غسيلThe product was then eluted from the silica with 10% methanol in ethyl acetate
- 10أخرىThe 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.