Reaktion #62376

ord-c6f74879b55d4a9f9448b3912936560b

Reaktionsgleichung

NS(=O)(=O)O
sulfamic acid
O=Cc1ccc(C(=O)OCc2ccccc2)o1
5-formylfuran-2-carboxylic acid benzyl ester
[Na+].[O-][Cl+][O-]
sodium chlorite
O=P([O-])(O)O.[K+]
potassium dihydrogen phosphate
O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulfate
O=C(O)c1ccc(C(=O)OCc2ccccc2)o1
title compound
Ausbeute 99.2%
O=C(O)c1ccc(C(=O)OCc2ccccc2)o1
Furan-2,5-dicarboxylic acid monobenzyl ester
Ausbeute 99.2%

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONadded with a solution
  2. 2
    workup.ADDITIONwas added dropwise
  3. 3
    TemperaturAfter cooling at this temperature for 30 minutes
  4. 4
    Sonstigethe reaction
  5. 5
    Extraktionextracted with a mixture of tetrahydrofuran and ethyl acetate
  6. 6
    WaschenThe organic phase was washed with water and saturated brine
  7. 7
    Trocknendried over anhydrous magnesium sulfate
  8. 8
    workup.DISTILLATIONThe solvent was distilled off

Vorschrift

490 mg of 5-formylfuran-2-carboxylic acid benzyl ester was dissolved in 10 mL of acetonitrile, and added with a solution containing 413 mg of sulfamic acid in 5 mL of water. After cooling to 0° C., a solution containing 202 mg of sodium chlorite and 232 mg of potassium dihydrogen phosphate in 5 mL of water was added dropwise. After cooling at this temperature for 30 minutes, sodium thiosulfate aqueous solution was added at 0° C. to stop the reaction, and extracted with a mixture of tetrahydrofuran and ethyl acetate. The organic phase was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to afford 520 mg of the title compound as white crystals.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07429609B2uspto-grants-2008_09