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

HRID 2276829
Notes
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Reaction equation

HRID 2276829 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

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

Product 1

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

Reagents, catalysts & solvents 3

HCID 11010647Acetylacetonatobis(ethylene)rhodium(I)Catalyst
HCID 962
Water
Solvent
HCID 312751,4-DioxaneSolvent

Procedure

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).

Workup

  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)

Sources & evidence

ORD record
ord-cd63ba525b9547de89a73930696a886b
Source dataset
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09133140B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes