Reacción #725896

ord-a64f066403194fab90fa2237b478c377

Ecuación de reacción

COC(=O)COCCBr
(2-bromoethoxy) acetic acid methyl ester
O=[N+]([O-])c1ccc(O)cc1
4-nitrophenol
O=C([O-])[O-].[K+].[K+]
K2CO3
[I-].[Na+]
sodium iodide
COC(=O)COCCOc1ccc([N+](=O)[O-])cc1
22
Rendimiento 43.6%
COC(=O)COCCOc1ccc([N+](=O)[O-])cc1
[2-(4-Nitrophenoxy)-ethoxy]acetic acid methyl ester
Rendimiento 43.6%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturarefluxed for 24 hours
  2. 2
    workup.DISTILLATIONAcetone was distilled off
  3. 3
    workup.ADDITIONwater (100 ml) was added
  4. 4
    FiltraciónCrude 22 was filtered
  5. 5
    Otrodried
  6. 6
    Otropurified by column chromatography on silica gel

Procedimiento

To a mixture of 4-nitrophenol (5 g, 36 mmol), anhydrous K2CO3 (20 g, 145 mmol) and sodium iodide (2 grams, 13.3 mmol) in anhydrous acetone (100 ml) was added (2-bromoethoxy) acetic acid methyl ester (11 g, 56 mmol) and refluxed for 24 hours. Acetone was distilled off and water (100 ml) was added. Crude 22 was filtered, dried and purified by column chromatography on silica gel using benzene as eluant to give pure 22 (4 g, 43.6%) as a white fluffy powder. The melting point was found to be 96-97.8° C. The structure was confirmed with IR and NMR.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07691364B2uspto-grants-2010_04