Reaktion #43433

ord-e1b48a1aa2ce41328b469642173ae43e

Reaktionsgleichung

C=Cc1cc2c(nn1)SCCO2
3-ethenyl-6,7-dihydro[1,4]oxathiino[3,2-c]pyridazine
[Na+].[O-][I+3]([O-])([O-])[O-]
sodium periodate
O=C([O-])O.[Na+]
sodium bicarbonate
O=Cc1cc2c(nn1)SCCO2
solid
Ausbeute 31.2%
O=Cc1cc2c(nn1)SCCO2
6,7-Dihydro[1,4]oxathiino[3,2-c]pyridazine-3-carbaldehyde
Ausbeute 31.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeevaporated to dryness
  2. 2
    workup.DISSOLUTIONdissolved in 1,4-dioxane
  3. 3
    workup.ADDITIONSilica gel was added
  4. 4
    Sonstigethe mixture was evaporated to dryness
  5. 5
    workup.ADDITIONadded to a silica column (20 g)
  6. 6
    Sonstigechromatographed
  7. 7
    Wascheneluting with 0-100% ethyl acetate in hexane

Vorschrift

A solution of 3-ethenyl-6,7-dihydro[1,4]oxathiino[3,2-c]pyridazine (200 mg, 1.11 mmol) in 1,4-dioxane/water (10 ml/2 ml) was treated with an aqueous solution of osmium tetroxide (4% w/v, 1 ml) and sodium periodate (0.55 g), initially stirred in an ice-bath for 1.5 hours, then allowed to warm to room temperature. After 1.5 hours the mixture was treated with sodium bicarbonate solution, evaporated to dryness and dissolved in 1,4-dioxane and chloroform. Silica gel was added and the mixture was evaporated to dryness, added to a silica column (20 g), and chromatographed, eluting with 0-100% ethyl acetate in hexane, to afford a pale yellow solid (63 mg, 31%).

Quelle

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