Reaktion #43450

ord-0b2aa9c7bc564ef3a9dc754bff5f9d20

Reaktionsgleichung

[Na+].[O-][I+3]([O-])([O-])[O-]
sodium periodate
C=Cc1cc2c(nn1)OCCO2
3-ethenyl-6,7-dihydro[1,4]dioxino[2,3-c]pyridazine
O=Cc1cc2c(nn1)OCCO2
solid
Ausbeute 64.4%
O=Cc1cc2c(nn1)OCCO2
6,7-Dihydro[1,4]dioxino[2,3-c]pyridazine-3-carbaldehyde
Ausbeute 64.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas evaporated to dryness
  2. 2
    Sonstigeazeotroped with 1,4-dioxane
  3. 3
    workup.ADDITIONSilica gel, 1,4-dioxane and chloroform were added
  4. 4
    Sonstigethe mixture was evaporated to dryness overnight
  5. 5
    workup.ADDITIONadded to a silica column (400 g)
  6. 6
    Sonstigechromatographed
  7. 7
    Wascheneluting with chloroform

Vorschrift

A solution of 3-ethenyl-6,7-dihydro[1,4]dioxino[2,3-c]pyridazine (11.58 g) in 1,4-dioxane/water (600 ml/180 ml), cooled in ice, was treated with an aqueous solution of osmium tetroxide (4% w/v, 25 ml) and sodium periodate (43 g). This mixture was allowed to warm to room temperature and after 7 hours under stirring the mixture was evaporated to dryness and azeotroped with 1,4-dioxane. Silica gel, 1,4-dioxane and chloroform were added and the mixture was evaporated to dryness overnight, then added to a silica column (400 g) and chromatographed, eluting with chloroform then 0-100% ethyl acetate in hexane, to afford a white solid (7.55 g, 64%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732460B2uspto-grants-2010_06