HCID 58502815, Verbindung → 2-(4'-Chloro-4-ethylbiphenyl-3-yl)cyclopent-4-ene-1,3-dione

HRID 40472Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 40472
CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.[Cl:14][C:15]1[CH:35]=[CH:34][C:18]([C:19]2[CH:20]=[CH:21][C:22]([CH2:32][CH3:33])=[C:23]([CH:25]3[C:29](=[O:30])[CH:28]=[CH:27][CH:26]3[OH:31])[CH:24]=2)=[CH:17][CH:16]=1>CC(C)=O>[Cl:14][C:15]1[CH:16]=[CH:17][C:18]([C:19]2[CH:20]=[CH:21][C:22]([CH2:32][CH3:33])=[C:23]([CH:25]3[C:29](=[O:30])[CH:28]=[CH:27][C:26]3=[O:31])[CH:24]=2)=[CH:34][CH:35]=1

Komponenten

4

Versuchsvorschrift

Jones' reagent (126 ml of 1.67 M solution, 210.4 mmol) prepared according to the procedure described above, is added dropwise over 30 minutes to a cooled (ice-bath) solution of 5-(4′-chloro-4-ethylbiphen-3-yl)-4-hydroxycyclopent-2-enone (59.84 g, 191.3 mmol) in acetone (615 ml). The mixture is stirred for 20 minutes, then the cooling bath is removed and the mixture is stirred for 1 hour at room temperature. Isopropanol (500 ml) is added to the yellow slurry and the mixture is stirred at room temperature for 2 hours. The mixture is diluted with ethyl acetate and washed with brine, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure to give 2-(4′-chloro-4-ethylbiphen-3-yl)cyclopent-4-ene-1,3-dione (47.94 g) as a yellow solid.

Aufarbeitung

  1. additionis added dropwise over 30 minutes to
  2. customthe cooling bath is removed
  3. stirringthe mixture is stirred for 1 hour at room temperature
  4. additionIsopropanol (500 ml) is added to the yellow slurry
  5. stirringthe mixture is stirred at room temperature for 2 hours
  6. additionThe mixture is diluted with ethyl acetate
  7. washwashed with brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. customthe filtrate is evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-985e93712e9c419b896505a938f71697
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08530388B2

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