تفاعل #1379894

ord-482c6df128214fafa7a89e416480c337

معادلة التفاعل

O
water
C=CC(=O)Cl
Acryloyl chloride
ClCCl
dichloromethane
NO
hydroxylamine
CN(O)[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
N-Methyl,N-(tert-butyldiphenylsilyl)hydroxylamine
ClCCl
dichloromethane
C=CC(=O)N(C)O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
N-Methyl,N-(tert-butyldiphenylsilyloxy)acrylamide

ظروف التفاعل

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

المعالجة

  1. 1
    workup.ADDITIONN,Ndiisopropylethylamine was added
  2. 2
    أخرىthe two layers were separated
  3. 3
    غسيلThe organic layer was washed with 10% ammonium chloride, saturated bicarbonate solution, and brine
  4. 4
    تجفيفThe organic solution was then dried with magnesium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    أخرىthe solvent evaporated under reduced pressure
  7. 7
    أخرىThe crude product was purified by flash chromatography (silica gel)
  8. 8
    workup.ADDITIONa mixture of hexane and ethyl acetate
  9. 9
    غسيلto elute the compound
  10. 10
    أخرىThe 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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07238339B2uspto-grants-2007_07