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N-Iodosuccinimide → 6-Chloro-4'-fluoro-4-iodobiphenyl-3-ol

HRID 1619704
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HRID 1619704 반응식
[Cl:1][C:2]1[C:7]([C:8]2[CH:13]=[CH:12][C:11]([F:14])=[CH:10][CH:9]=2)=[CH:6][C:5]([OH:15])=[CH:4][CH:3]=1.[I:16]N1C(=O)CCC1=O>C(O)(=O)C.ClCCl.S(=O)(=O)(O)O>[Cl:1][C:2]1[C:7]([C:8]2[CH:13]=[CH:12][C:11]([F:14])=[CH:10][CH:9]=2)=[CH:6][C:5]([OH:15])=[C:4]([I:16])[CH:3]=1
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참가 물질

6

반응물 2

HCID 120273N-IodosuccinimideHCID 580423356-Chloro-4'-fluorobiphenyl-3-ol

생성물 1

HCID 580423526-Chloro-4'-fluoro-4-iodobiphenyl-3-ol수율 72.6%

시약·촉매·용매 3

HCID 176Acetic Acid용매HCID 1118Sulfuric Acid용매HCID 6344Dichloromethane용매
2회

실험 절차

To a solution of 6-chloro-4′-fluorobiphenyl-3-ol (Preparation 104, 280 mg, 1.26 mmol) in acetic acid (2.5 mL), dichloromethane (2.5 mL) and concentrated sulfuric acid (25 μL) was added N-iodosuccinimide (272 mg, 1.21 mmol) at room temperature. The reaction mixture was stirred for 18 hours at room temperature. Dichloromethane (60 mL) was added and the organic layer was washed with brine (2×20 mL), dried over MgSO4, filtered and evaporated. The residue was purified by silica gel chromatography eluting 33% dichloromethane in heptane to afford the title compound (306 mg, 70%) as a colourless oil.

후처리

  1. washthe organic layer was washed with brine (2×20 mL)
  2. dry with materialdried over MgSO4
  3. filtrationfiltered
  4. customevaporated
  5. customThe residue was purified by silica gel chromatography
  6. washeluting 33% dichloromethane in heptane

출처 및 근거

ORD 기록
ord-4f3c67bb21404cebbf74b251aa3201e6
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772293B2

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