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Trichloroacetyl chloride → (RS)-3-benzyl-2,2-dichlorocyclobutanone

HRID 1280750
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HRID 1280750 반응식
[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[CH:2]=[CH2:3].[Cl:10][C:11]([Cl:16])(Cl)[C:12](Cl)=[O:13].P(Cl)(Cl)(Cl)=O>C(OCC)C.[Cu].[Zn]>[CH2:1]([CH:2]1[CH2:3][C:12](=[O:13])[C:11]1([Cl:16])[Cl:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
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참가 물질

6

반응물 3

HCID 6420Trichloroacetyl chlorideHCID 9309AllylbenzeneHCID 24813Phosphorus oxychloride

생성물 1

HCID 18425787(RS)-3-benzyl-2,2-dichlorocyclobutanone수율 20%

시약·촉매·용매 2

HCID 10290809Zinc copper couple촉매HCID 3283Diethyl Ether용매2회

실험 절차

To a room temperature mixture containing allylbenzene (1.84 g, 15.6 mmol), zinc-copper couple (5.1 g, 78 mmol) and diethylether (60 ml) was added dropwise a solution of trichloroacetylchloride (2.96 ml, 26.5 mmol) and phosphorus oxychloride (2.46 ml, 26.5 mmol) in diethylether (20 ml). The reaction mixture was stirred at room temperature for 1 hour, filtered and the filtrate was partially concentrated. The residue was neutralized with saturated NaHCO3. The aqueous phase was extracted with diethylether. The combined organic phases were washed successively with H2O and brine, dried over Na2SO4, and concentrated. The residue was chromatographed over silica gel (hexane) to provide (RS)-3-benzyl-2,2-dichlorocyclobutanone (0.71 g, 20%) as a yellow oil, MS: m/e=228.1 (M-H+).

후처리

  1. filtrationfiltered
  2. concentrationthe filtrate was partially concentrated
  3. extractionThe aqueous phase was extracted with diethylether
  4. washThe combined organic phases were washed successively with H2O and brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated
  7. customThe residue was chromatographed over silica gel (hexane)

출처 및 근거

ORD 기록
ord-aed1c7b77c754df9b4747f0e8f78d895
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06451819B2

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