تفاعل #1379894
ord-482c6df128214fafa7a89e416480c337
معادلة التفاعل
المتفاعلات
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المعالجة
- 1workup.ADDITIONN,Ndiisopropylethylamine was added
- 2أخرىthe two layers were separated
- 3غسيلThe organic layer was washed with 10% ammonium chloride, saturated bicarbonate solution, and brine
- 4تجفيفThe organic solution was then dried with magnesium sulfate
- 5ترشيحfiltered
- 6أخرىthe solvent evaporated under reduced pressure
- 7أخرىThe crude product was purified by flash chromatography (silica gel)
- 8workup.ADDITIONa mixture of hexane and ethyl acetate
- 9غسيلto elute the compound
- 10أخرىThe purification
الإجراء التجريبي
Dry dichloromethane (50 mL) was added to N-Methyl,N-(tert-butyldiphenylsilyl)hydroxylamine to dissolve the hydroxylamine derivative. N,Ndiisopropylethylamine was added. The resulting solution was stirred and cooled at 0° C. with an ice bath. Acryloyl chloride in 10 mL of dry dichloromethane was added. Then water was added and the two layers were separated. The organic layer was washed with 10% ammonium chloride, saturated bicarbonate solution, and brine. The organic solution was then dried with magnesium sulfate, filtered, and the solvent evaporated under reduced pressure. The crude product was purified by flash chromatography (silica gel) using a mixture of hexane and ethyl acetate to elute the compound. The purification produced N-Methyl,N-(tert-butyldiphenylsilyloxy)acrylamide (28).