Reaktion #42015

ord-bd280309d1274ad4b0b18844835c296f

Reaktionsgleichung

[Na+].[O-][Br+2]([O-])[O-]
sodium bromate
OCc1ccccc1
benzyl alcohol
CCOCC
ether
O=C(O)c1ccccc1
benzoic acid
Ausbeute 90.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    Filtrationthe catalyst was filtered off
  3. 3
    SonstigeThe organic layer was separated
  4. 4
    Extraktionthe aqueous phase was extracted with ether (2×50 ml)
  5. 5
    WaschenThe combined organic extracts were washed with water (25 ml)
  6. 6
    Trocknendried with anhydrous magnesium sulphate
  7. 7
    Einengenconcentrated

Vorschrift

A mixture of Ceiv catalyst from Example 47 (0.08 g), sodium bromate (0.3 g) and benzyl alcohol (0.216 g, 2 mmol) in acetonitrile:water (5:7, 12 ml) was stirred at 80° C. for 40 h under an atmosphere of nitrogen. On cooling ether (70 ml) was added and the catalyst was filtered off. The organic layer was separated and the aqueous phase was extracted with ether (2×50 ml). The combined organic extracts were washed with water (25 ml), dried with anhydrous magnesium sulphate and concentrated to give benzoic acid as a white solid (0.22 g, 90%). M.p. 120° C., lit. 120-122° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728159B2uspto-grants-2010_06