تفاعل #1922

ord-08ed9fc621264a2f9632e16668245bd7

معادلة التفاعل

O=C([O-])O.[Na+]
sodium bicarbonate
COC(=O)c1ccccc1CBr
methyl 2-bromomethylbenzoate
CC(=O)Nc1cccc(O)c1
3-acetamidophenol
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
COC(=O)c1ccccc1COc1cccc(NC(C)=O)c1
methyl 2-(3-acetamidophenoxymethyl)benzoate
المردود 61.2%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred overnight at room temperature
  2. 2
    استخلاصfollowed by extraction with ethyl acetate
  3. 3
    غسيلThe organic layer was washed with a saturated aqueous solution of sodium chloride
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    ترشيحAfter the drying agent was filtered off
  6. 6
    تركيزthe organic layer was concentrated under reduced pressure
  7. 7
    أخرىThe obtained oily substance was purified by silica gel column chromatography (hexane/ethyl acetate=4/1)

الإجراء التجريبي

To a solution of 3-acetamidophenol (1.0 g, 6.6 mmol) in dimethylformamide (10 ml) was added cesium carbonate (1.3 g, 3.9 mmol), followed by stirring at room temperature for 30 minutes. To the resulting mixture was added methyl 2-bromomethylbenzoate (1.8 g, 7.9 mmol), and the mixture was stirred overnight at room temperature. After the reaction was completed, the reaction mixture was poured into a5% aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the organic layer was concentrated under reduced pressure. The obtained oily substance was purified by silica gel column chromatography (hexane/ethyl acetate=4/1), followed by trituration with hexane to give methyl 2-(3-acetamidophenoxymethyl)benzoate as a white solid (1.21 g, 61%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726325uspto-grants-1998_03