Acetone → 7-fluoro-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one

HRID 490955

Reaktionsgleichung

Reaktionsgleichung von HRID 490955
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[C:4]([OH:11])[CH:3]=1.[CH3:12][C:13]([CH3:15])=O.N1CCCC1>C1C=CC=CC=1>[F:1][C:2]1[CH:3]=[C:4]2[C:5]([C:8](=[O:10])[CH2:9][C:13]([CH3:15])([CH3:12])[O:11]2)=[CH:6][CH:7]=1

Komponenten

5

Edukt 3

HCID 180AcetoneHCID 31268PyrrolidineHCID 27373264'-Fluoro-2'-hydroxyacetophenone

Produkt 1

HCID 152053737-fluoro-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-oneAusbeute 53 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

1-(4-Fluoro-2-hydroxy-phenyl)-ethanone (5.0 g, 32.44 mmol), acetone (11.92 mL, 162.2 mmol) and pyrrolidine (2.7 mL, 32.44 mmol) were dissolved in 20 mL benzene, and the reaction mixture was refluxed for four hours. The reaction mixture was cooled to room temperature and partitioned between ethyl acetate and 1 N HCl. The organic layer was dried over MgSO4, and solvent was evaporated under reduced pressure. The resulting residue was chromatographed (15% ethyl acetate in hexanes eluting through silica) and solvent was removed to yield 3.33 g (17.16 mg, 53%) of 7-fluoro-2,2-dimethyl-chroman-4-one as an oil. MS: 195 (M+H)+.

Aufarbeitung

  1. temperaturethe reaction mixture was refluxed for four hours
  2. custompartitioned between ethyl acetate and 1 N HCl
  3. dry with materialThe organic layer was dried over MgSO4, and solvent
  4. customwas evaporated under reduced pressure
  5. customThe resulting residue was chromatographed (15% ethyl acetate in hexanes eluting through silica) and solvent
  6. customwas removed

Quellen und Nachweise

ORD-Eintrag
ord-4df5a3bcc2434497a2a7b54276b5a6ba
Quelldatensatz
uspto-grants-2009_05
Patentnummer
US07528250B2

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