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N-碘代丁二酰亚胺 → 6-Chloro-4'-fluoro-4-iodobiphenyl-3-ol

HRID 1619704
笔记
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反应方程式

HRID 1619704 反应方程式
[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
参与物实验过程后处理来源与证据反应笔记

参与物

6

反应物 2

HCID 120273N-碘代丁二酰亚胺HCID 580423356-Chloro-4'-fluorobiphenyl-3-ol

产物 1

HCID 580423526-Chloro-4'-fluoro-4-iodobiphenyl-3-ol收率 72.6%

试剂、催化剂与溶剂 3

HCID 176醋酸溶剂HCID 1118四氧化硫溶剂HCID 6344二氯甲烷溶剂2 次

实验过程

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.

后处理

  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

来源与证据

ORD记录
ord-4f3c67bb21404cebbf74b251aa3201e6
来源数据集
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08772293B2

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记