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Ethyl Acetate → 4-Bromo-2-cyclobutylphenol

HRID 522263
ノート
印刷プレビュー

反応式

HRID 522263 の反応式
[Br-:1].[Br-].[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC.[CH:55]1([C:59]2[CH:64]=[CH:63][CH:62]=[CH:61][C:60]=2[OH:65])[CH2:58][CH2:57][CH2:56]1.S([O-])([O-])=O.[Na+].[Na+].CCOC(C)=O>C(Cl)Cl>[Br:1][C:63]1[CH:62]=[CH:61][C:60]([OH:65])=[C:59]([CH:55]2[CH2:56][CH2:57][CH2:58]2)[CH:64]=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 4

HCID 8857Ethyl AcetateHCID 24437Sodium SulfiteHCID 128063072-CyclobutylphenolHCID 23500184Tetra-n-butylammonium tribromide

生成物 1

HCID 900655734-Bromo-2-cyclobutylphenol収率 166.9%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane
溶媒

実験手順

Tetra-n-butylammonium tribromide (4.72 g) was added to a solution of 2-cyclobutylphenol (1.21 g) in CH2Cl2 (24.2 mL) at room temperature, and the mixture was stirred at the same temperature overnight. After the reaction mixture was pour into a saturated aqueous sodium sulfite solution, extraction was performed on the mixture using EtOAc, and the extract was washed with water and saturated brine. The organic layer was dried over Na2SO4 and filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Hex:EtOAc=100:0 to 84:16), whereby 4-bromo-2-cyclobutylphenol (1.85 g) was obtained as a colorless oil.

後処理

  1. washthe extract was washed with water and saturated brine
  2. dry with materialThe organic layer was dried over Na2SO4
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (Hex:EtOAc=100:0 to 84:16)

出典と根拠

ORDレコード
ord-53386a26e45347309ba3293097c0b50a
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09328118B2

反応ノート

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