Reaktion #1461802

ord-7bd4349184534901926b1f62c5132dce

Reaktionsgleichung

CI
methyl iodide
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CC(C)(CC(C(=O)c1ccccc1)c1ccco1)c1cc(F)ccc1Br
2-[1-benzoyl-3-(2-bromo-5-fluorophenyl)-3-methylbutyl]furan
O=S([O-])[O-].[Na+].[Na+]
Na2SO3
O=C(O)CC(O)(CC(=O)O)C(=O)O
citric acid
[Na+].[O-][I+3]([O-])([O-])[O-]
sodium periodate
COC(=O)C(CC(C)(C)c1cc(F)ccc1Br)C(=O)c1ccccc1
product
COC(=O)C(CC(C)(C)c1cc(F)ccc1Br)C(=O)c1ccccc1
2-Benzoyl-4-(2-bromo-5-fluorophenyl)-4-methylvaleric acid-methyl ester

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe batch is extracted with ethyl acetate
  2. 2
    TrocknenThe combined extracts are dried (Na2SO4)
  3. 3
    Einengenconcentrated by evaporation in a vacuum
  4. 4
    workup.WAITAfter 5 hours at room temperature
  5. 5
    Waschenwashed with 10% sulfuric acid and saturated NaCl
  6. 6
    Trocknendried (Na2SO4)
  7. 7
    Einengenconcentrated by evaporation in a vacuum

Vorschrift

A suspension of 10.9 g (50.8 mmol) of sodium periodate in 140 ml of water-acetonitrile-tetrachloromethane (4:2:1) is mixed with 45 mg (0.34 mmol) of ruthenium(IV)oxide-hydrate. After 10 minutes, a solution of 2-[1-benzoyl-3-(2-bromo-5-fluorophenyl)-3-methylbutyl]furan in 40 ml of acetonitrile is added to it, it is stirred for another 10 minutes, and the batch is poured into 400 ml of saturated Na2SO3. A pH of 5 is set with 10% citric acid, and the batch is extracted with ethyl acetate. The combined extracts are dried (Na2SO4) and concentrated by evaporation in a vacuum. The residue is taken up in 8 ml of DMF and treated with 0.42 ml (6.8 mmol) of methyl iodide and 2.21 g (6.8 mmol) of cesium carbonate. After 5 hours at room temperature, the batch is diluted with 600 ml of MTBE, washed with 10% sulfuric acid and saturated NaCl, dried (Na2SO4) and concentrated by evaporation in a vacuum. Column chromatography on silica gel with hexane-ethyl acetate yields 0.9 g of product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07166592B2uspto-grants-2007_01