Cesium carbonate → 2-Diazoindane-1,3-dione

HRID 1243344Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1243344
[N-]=[N+:2]=[N-:3].[Na+].CS(Cl)(=O)=O.[C:10]1(=[O:20])[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[C:12](=[O:19])[CH2:11]1.C(=O)([O-])[O-].[Cs+].[Cs+]>CC#N>[N+:2](=[C:11]1[C:10](=[O:20])[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[C:12]1=[O:19])=[N-:3]

Komponenten

6

Versuchsvorschrift

To a suspension of sodium azide (2.4 g, 36.3 mmol) in CH3CN (73 mL) was added methanesulfonyl chloride (2.8 mL, 36.3 mmol). After stirring for 16 h, the reaction mixture was poured over a suspension of indan-1,3-dione (5.3 g, 36.3 mmol) and cesium carbonate (11.8 g, 36.3 mmol) in CH3CN (50 mL). The mixture was stirred until reaction was complete (2 h), and then filtered through Celite. The filter cake was washed with EtOAc and the organic solvents were removed in vacuo. The resulting gum was diluted with EtOAc and rinsed successively with NaOH (1N), H2O and brine. The organic layer was dried (MgSO4), evaporated and the crude oil purified by flash chromatography (SiO2, 50% hexane/EtOAc) to give 2-diazoindan-1,3-dione (2a) (2.6 g, 42% yield).

Aufarbeitung

  1. stirringThe mixture was stirred until reaction
  2. custom(2 h)
  3. filtrationfiltered through Celite
  4. washThe filter cake was washed with EtOAc
  5. customthe organic solvents were removed in vacuo
  6. additionThe resulting gum was diluted with EtOAc
  7. washrinsed successively with NaOH (1N), H2O and brine
  8. dry with materialThe organic layer was dried (MgSO4)
  9. customevaporated
  10. customthe crude oil purified by flash chromatography (SiO2, 50% hexane/EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-0c7fea602f584edda0ca346530acf2f6
Quelldatensatz
uspto-grants-2006_10
Patentnummer
US07119099B2

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