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2-Cyclopenten-1-one → (R)-3-(3-Bromophenyl)cyclopentan-1-one

HRID 2276829
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2276829
[Br:1][C:2]1[CH:3]=[C:4](OB(O)O)[CH:5]=[CH:6][CH:7]=1.[C:12]1(=[O:17])[CH2:16][CH2:15][CH:14]=[CH:13]1.C(=O)(O)[O-].[Na+]>O1CCOCC1.O.C/C(/O)=C/C(C)=O.C=C.C=C.[Rh]>[Br:1][C:2]1[CH:3]=[C:4]([C@@H:14]2[CH2:15][CH2:16][C:12](=[O:17])[CH2:13]2)[CH:5]=[CH:6][CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 135882-Cyclopenten-1-oneHCID 516892Sodium BicarbonateHCID 183739503-Bromophenylboric acid

Produkt 1

HCID 67296121(R)-3-(3-Bromophenyl)cyclopentan-1-oneAusbeute 102 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 11010647Acetylacetonatobis(ethylene)rhodium(I)Katalysator
HCID 962
Water
Lösungsmittel
HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

Under a nitrogen stream, 3-bromophenylboric acid (14.2 g, 71 mmol), (R)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl((R)-BINAP) (1.06 g, 1.7 mmol), and acetylacetonato bis(ethylene)rhodium(I) (438 mg, 1.7 mmol) were dissolved in a solvent mixture of 1,4-dioxane (150 mL) and water (15 mL), followed by degassing with ultrasonic waves, and then cyclopentenone (2.4 mL, 28 mmol) was added and the mixture was stirred under reflux with heating for 3 hours. The reaction solution was cooled to room temperature, followed by addition of saturated aqueous sodium bicarbonate solution, and then the solvent was distilled off under reduced pressure. The aqueous phase was extracted with ethyl acetate, the organic phase was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue obtained was purified by column chromatography (ethyl acetate/hexane:10/90-20/80) to give the title compound (6.83 g).

Aufarbeitung

  1. customby degassing with ultrasonic waves
  2. temperatureunder reflux
  3. temperaturewith heating for 3 hours
  4. distillationthe solvent was distilled off under reduced pressure
  5. extractionThe aqueous phase was extracted with ethyl acetate
  6. dry with materialthe organic phase was dried over anhydrous magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure
  8. customThe residue obtained
  9. customwas purified by column chromatography (ethyl acetate/hexane:10/90-20/80)

Quellen und Nachweise

ORD-Eintrag
ord-cd63ba525b9547de89a73930696a886b
Quelldatensatz
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09133140B2

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