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Thionyl Chloride → 6-bromo-4,7-difluoro-2,3-dihydro-1H-inden-1-one

HRID 533940
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 533940
[Br:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([CH2:9][CH2:10][C:11]([OH:13])=O)=[C:4]([F:14])[CH:3]=1.O=S(Cl)Cl.[Al+3].[Cl-].[Cl-].[Cl-]>C(Cl)Cl>[Br:1][C:2]1[C:7]([F:8])=[C:6]2[C:5]([CH2:9][CH2:10][C:11]2=[O:13])=[C:4]([F:14])[CH:3]=1
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Komponenten

5

Edukt 3

HCID 24386Thionyl ChlorideHCID 6451240Aluminum(III) ChlorideHCID 848075163-(4-Bromo-2,5-difluorophenyl)propanoic acid

Produkt 1

HCID 867151266-bromo-4,7-difluoro-2,3-dihydro-1H-inden-1-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of 3-(4-bromo-2,5-difluorophenyl)propanoic acid (1.10 g) in DCM (20 mL) was added SOCl2 (2.45 g). The mixture was stirred at room temperature for 18 hours. The solvent was removed by evaporation under reduced pressure. The residue was dried under high vacuum to give a crude solid. To the residue was added AlCl3 (2.76 g) and the mixture heated to 130° C. The mixture was stirred at 130° C. for 2 hours and then cooled to room temperature. The resulting mixture was treated with ice water and then extracted with ethyl acetate (50 mL×3). The organic phase was washed with brine, dried over Na2SO4, and concentrated. The residue was purified by silica gel column chromatography eluting with petroleum ether/ethyl acetate (5:1) to give the subtitle compound as a light yellow solid. MS ESI+: m/z=247 [M+H]+.

Aufarbeitung

  1. customThe solvent was removed by evaporation under reduced pressure
  2. customThe residue was dried under high vacuum
  3. customto give a crude solid
  4. temperaturethe mixture heated to 130° C
  5. stirringThe mixture was stirred at 130° C. for 2 hours
  6. temperaturecooled to room temperature
  7. extractionextracted with ethyl acetate (50 mL×3)
  8. washThe organic phase was washed with brine
  9. dry with materialdried over Na2SO4
  10. concentrationconcentrated
  11. customThe residue was purified by silica gel column chromatography
  12. washeluting with petroleum ether/ethyl acetate (5:1)

Quellen und Nachweise

ORD-Eintrag
ord-ac3cfeb9e10c40eaaee881c3407cd308
Quelldatensatz
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08853412B2

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