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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Cyclopenten-1-one → (R)-3-(3-Bromophenyl)cyclopentan-1-one

HRID 2276829
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HRID 2276829 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

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

생성물 1

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

시약·촉매·용매 3

HCID 11010647Acetylacetonatobis(ethylene)rhodium(I)촉매HCID 962
Water
용매
HCID 312751,4-Dioxane용매

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-cd63ba525b9547de89a73930696a886b
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133140B2

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