تفاعل #974971

ord-436f9e75fb664518b753e96e29d5e918

الكواشف

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المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe organic solvent was evaporated under reduced pressure
  2. 2
    workup.ADDITIONThe residual aqueous solution was diluted with saturated aqueous sodium hydrogen carbonate solution
  3. 3
    استخلاصthe mixture was extracted with ethyl acetate
  4. 4
    غسيلThe extract was washed with saturated brine
  5. 5
    تجفيفdried over anhydrous sodium sulfate
  6. 6
    أخرىThe solvent was evaporated under reduced pressure
  7. 7
    أخرىthe residue was purified by silica gel column chromatography (NH, ethyl acetate)

الإجراء التجريبي

To a solution of methyl 3-amino-6-bromo-5-chloro-2-methylbenzoate (500 mg, 1.80 mmol) in acetic acid (9 mL) was added a solution of sodium nitrite (137 mg, 1.99 mmol) in water (0.9 mL) at room temperature, and the mixture was stirred for 24 hr. The organic solvent was evaporated under reduced pressure. The residual aqueous solution was diluted with saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, ethyl acetate) to give the title compound (398 mg, yield 76%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08247429B2uspto-grants-2012_08