Sodium periodate → HCID 13656093, Verbindung

HRID 745990

Reaktionsgleichung

Reaktionsgleichung von HRID 745990
[Br:1][C:2]1[C:3]([S:18][CH2:19][C:20]([OH:22])=[O:21])=[CH:4][C:5]2[O:9][N:8]=[C:7]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[F:16])[C:6]=2[CH:17]=1.I([O-])(=O)(=O)=[O:24].[Na+].I([O-])(=O)=O.[Na+]>CO.O>[Br:1][C:2]1[C:3]([S:18]([CH2:19][C:20]([OH:22])=[O:21])=[O:24])=[CH:4][C:5]2[O:9][N:8]=[C:7]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[F:16])[C:6]=2[CH:17]=1

Komponenten

5

Versuchsvorschrift

2.8 g (7.33 mmol) of [[5-bromo-3-(2-fluorophenyl)-1,2-benzisoxazol-6-yl]thio]acetic acid was combined with 30 ml (2 eq.) of 0.5M sodium periodate solution in 300 ml of 4:1 methanol/water. The mixture was refluxed for 18 hours during which the insoluble sodium iodate precipitated. The reaction mixture was then poured into excess 3N HCl and extracted several times with ethyl acetate. The ethyl acetate extracts were combined, washed with water and a saturated salt solution, dried over magnesium sulfate, filtered and evaporated to yield a white solid. The solid was triturated with hexanes and dried under vacuum to yield 2.51 g (86%) of [[5-bromo-3-(2-fluorophenyl)-1,2-benzisoxazol-6-yl]sulfinyl]acetic acid, m.p. 173°-174° C.

Aufarbeitung

  1. customprecipitated
  2. additionThe reaction mixture was then poured into excess 3N HCl
  3. extractionextracted several times with ethyl acetate
  4. washwashed with water
  5. dry with materiala saturated salt solution, dried over magnesium sulfate
  6. filtrationfiltered
  7. customevaporated
  8. customto yield a white solid
  9. customThe solid was triturated with hexanes
  10. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-42044842e9be46829554263d589b9a3d
Quelldatensatz
uspto-grants-1986_07
Patentnummer
US04602028

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