Water → Dibenzo[a,e]cyclopropa[c]cyclohepten-6(1H)-one, 1,1-difluoro-1a,10b-dihydro-

HRID 413954

Reaktionsgleichung

Reaktionsgleichung von HRID 413954
Cl[C:2]([F:7])([F:6])[C:3]([O-])=O.[Na+].[CH:9]1[C:19]2[CH:18]=C[C:16]3[CH:20]=[CH:21][CH:22]=[CH:23][C:15]=3[C:14](=[O:24])[C:13]=2[CH:12]=[CH:11][CH:10]=1.O>COCCOCCOC>[F:6][C:2]1([F:7])[CH:18]2[CH:3]1[C:23]1[CH:22]=[CH:21][CH:20]=[CH:16][C:15]=1[C:14](=[O:24])[C:13]1[CH:12]=[CH:11][CH:10]=[CH:9][C:19]=12

Komponenten

5

Edukt 3

HCID 962WaterHCID 166795H-Dibenzo[a,d]cyclohepten-5-oneHCID 2734985Sodium chlorodifluoroacetate

Produkt 1

HCID 12073911Dibenzo[a,e]cyclopropa[c]cyclohepten-6(1H)-one, 1,1-difluoro-1a,10b-dihydro-Ausbeute 45,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8150DiglymeLösungsmittel2×

Versuchsvorschrift

A solution of sodium chlorodifluoroacetate (350 g) in diglyme (1400 mL) was added dropwise over 4 to 8 hours, preferably over 6 hours, to a solution of 5H-dibenzo[a,d]cyclo-hepten-5-one (25 g) in diglyme (500 mL), with stirring, and under nitrogen, maintaining the reaction temperature at 160°-165° C. The cooled reaction mixture was poured into water (1.8 L) and extracted with ether (1.8 L). The organic phase was washed with water, dried over sodium sulfate (Na2SO4), and evaporated. The residue was recrystallized from ethanol, then from acetone/hexane to give 14 g of 1,1-difluoro-1a,10b-dihydrodibenzo[a,e]cyclopropa[c]-cyclohepten-6(1H)-one.

Aufarbeitung

  1. temperatureunder nitrogen, maintaining the reaction temperature at 160°-165° C
  2. customThe cooled reaction mixture
  3. extractionextracted with ether (1.8 L)
  4. washThe organic phase was washed with water
  5. dry with materialdried over sodium sulfate (Na2SO4)
  6. customevaporated
  7. customThe residue was recrystallized from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-3f71e71360174d3cbbbe18cf89673b84
Quelldatensatz
uspto-grants-2003_05
Patentnummer
US06570016B1

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