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

HRID 1280750
ノート
印刷プレビュー

反応式

HRID 1280750 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6420Trichloroacetyl chlorideHCID 9309AllylbenzeneHCID 24813Phosphorus oxychloride

生成物 1

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

試薬・触媒・溶媒 2

HCID 10290809Zinc copper couple触媒HCID 3283Diethyl Ether溶媒2 回

実験手順

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+).

後処理

  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)

出典と根拠

ORDレコード
ord-aed1c7b77c754df9b4747f0e8f78d895
出典データセット
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06451819B2

反応ノート

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