Reaktion #450048

Reaktionsgleichung

(E)-2-(3-((tert-butyldimethylsilyl)oxy)-6-fluoro-1-indanylidene) acetamide

pyridinium p-toluenesulfonate

→

(E)-2-(6-fluoro-3-hydroxy-1-indanylidene)acetamide

Ausbeute 62.1%

Lösungsmittel

ethanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeevaporated in vacuo
2. 2
   workup.DISSOLUTIONThe residue was dissolved in ethyl acetate (150 mL)
3. 3
   Waschenwashed successively with water (2×150 mL) and brine (150 mL)
4. 4
   Trocknendried over magnesium sulfate
5. 5
   Filtrationfiltered
6. 6
   Sonstigeevaporated in vacuo
7. 7
   SonstigeThe residue was chromatographed on silica gel eluting with ethyl acetate
8. 8
   Temperaturgradually increasing the polarity to ethyl acetate: ethanol (95:5)
9. 9
   workup.ADDITIONThe fractions containing the major spot
10. 10
    Sonstigeevaporated in vacuo
11. 11
    Sonstigethe residue was dried in a vacuum at 80° C. for 18 hours

Vorschrift

A solution of (E)-2-(3-((tert-butyldimethylsilyl)oxy)-6-fluoro-1-indanylidene) acetamide (1.80 g, 5.6 mmoles) and pyridinium p-toluenesulfonate (0.85 g, 3.4 mmoles, Aldrich) in ethanol (65 mL) was heated at 55°-68° C. for 3.5 hours under a nitrogen atmosphere and evaporated in vacuo. The residue was dissolved in ethyl acetate (150 mL) and washed successively with water (2×150 mL) and brine (150 mL), dried over magnesium sulfate, filtered and evaporated in vacuo. The residue was chromatographed on silica gel eluting with ethyl acetate, gradually increasing the polarity to ethyl acetate: ethanol (95:5). The fractions containing the major spot were combined and evaporated in vacuo, and the residue was dried in a vacuum at 80° C. for 18 hours to give 0.72 g (62%) of (E)-2-(6-fluoro-3-hydroxy-1-indanylidene)acetamide as a white solid, mp 166°-168° C.;

Quelle