Chloride → 5-fluoro-2,2,7-trimethylbenzofuran-3(2H)-one

HRID 1876398Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1876398
[F:1][C:2]1[CH:14]=[CH:13][C:5]([O:6][C:7]([CH3:12])([CH3:11])[C:8]([OH:10])=O)=[C:4]([CH3:15])[CH:3]=1.CN(C=O)C.[Cl-].[Al+3].[Cl-].[Cl-].[Cl-]>O1CCCC1>[F:1][C:2]1[CH:3]=[C:4]([CH3:15])[C:5]2[O:6][C:7]([CH3:12])([CH3:11])[C:8](=[O:10])[C:13]=2[CH:14]=1

Komponenten

6

Edukt 4

HCID 312ChlorideHCID 6228DimethylformamideHCID 6451240Aluminum(III) ChlorideHCID 585663572-(4-Fluoro-2-methylphenoxy)-2-methylpropanoic acid

Produkt 1

HCID 585662995-fluoro-2,2,7-trimethylbenzofuran-3(2H)-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoic acid (658) (5 g, 23.6 mmol) in tetrahydrofuran (50 mL) at 0° C. was added cat. DMF and oxayl chloride (2.5 mL, 28.3 mmol). The reaction was warmed to room temperature, stirred for 1 hour, and concentrated in vacuo. The oil was dissolved in dichloromethane (50 mL), cooled to −78° C. and AlCl3 (7.6 g, 56.6 mmol) was added. The reaction was allowed to warm to room temperature overnight. Ice water was added and the dichloromethane was removed in vacuo. The aqueous phase was extracted with ethyl acetate (3×50 mL) and washed with saturated sodium bicarbonate dried over sodium sulfate, filtered and concentrated in vacuo. The crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (20%) to provide 5-fluoro-2,2,7-trimethylbenzofuran-3(2H)-one (659).

Aufarbeitung

  1. concentrationconcentrated in vacuo
  2. dissolutionThe oil was dissolved in dichloromethane (50 mL)
  3. temperaturecooled to −78° C.
  4. temperatureto warm to room temperature overnight
  5. customthe dichloromethane was removed in vacuo
  6. extractionThe aqueous phase was extracted with ethyl acetate (3×50 mL)
  7. washwashed with saturated sodium bicarbonate
  8. dry with materialdried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. customThe crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (20%)

Quellen und Nachweise

ORD-Eintrag
ord-b3a4d63bd8754d23929b62a5e50b22b9
Quelldatensatz
uspto-grants-2012_11
Patentnummer
US08309600B2

Notizen zur Reaktion

Wird geladen…