Réaction #43431

ord-00096b25ac0a4aa5bdd47d8da325db37

Équation de réaction

C=Cc1cc2c(nn1)OCCS2
3-ethenyl-6,7-dihydro[1,4]oxathiino[2,3-c]pyridazine
[Na+].[O-][I+3]([O-])([O-])[O-]
sodium periodate
O=Cc1cc2c(nn1)OCCS2
solid
Rendement 36.0%
O=Cc1cc2c(nn1)OCCS2
6,7-Dihydro[1,4]oxathiino[2,3-c]pyridazine-3-carbaldehyde
Rendement 36.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreAfter 2.5 hours the mixture was evaporated to dryness
  2. 2
    workup.DISSOLUTIONdissolved in 1,4-dioxane
  3. 3
    workup.ADDITIONSilica gel was added
  4. 4
    Autrethe mixture was evaporated to dryness
  5. 5
    workup.ADDITIONadded to a silica column (50 g)
  6. 6
    Autrechromatographed
  7. 7
    Lavageeluting with 0-100% ethyl acetate in hexane

Mode opératoire

A solution of 3-ethenyl-6,7-dihydro[1,4]oxathiino[2,3-c]pyridazine (320 mg) in 1,4-dioxane/water (20 ml/5 ml) was treated with an aqueous solution of osmium tetroxide (4% w/v, 2 ml) and sodium periodate (1.08 g), initially stirred in an ice-bath, then allowed to warm to room temperature. After 2.5 hours the mixture was 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 (50 g) and chromatographed, eluting with 0-100% ethyl acetate in hexane, to afford a white solid (116 mg, 36%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07732460B2uspto-grants-2010_06