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

HRID 2276829
ノート
印刷プレビュー

反応式

HRID 2276829 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 3

HCID 11010647Acetylacetonatobis(ethylene)rhodium(I)触媒HCID 962Water
溶媒
HCID 312751,4-Dioxane溶媒

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-cd63ba525b9547de89a73930696a886b
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09133140B2

反応ノート

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