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N-Iodosuccinimide → 1-(5-Chloro-4-fluoro-2-hydroxy-3-iodophenyl)ethanone

HRID 626827
ノート
印刷プレビュー

反応式

HRID 626827 の反応式
[Cl:1][C:2]1[C:3]([F:12])=[CH:4][C:5]([OH:11])=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1.[I:13]N1C(=O)CCC1=O>C(O)(=O)C>[Cl:1][C:2]1[C:3]([F:12])=[C:4]([I:13])[C:5]([OH:11])=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 120273N-IodosuccinimideHCID 162214361-(5-Chloro-4-fluoro-2-hydroxyphenyl)ethanone

生成物 1

HCID 866668571-(5-Chloro-4-fluoro-2-hydroxy-3-iodophenyl)ethanone

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
70 °C

実験手順

A solution of 1-(5-chloro-4-fluoro-2-hydroxyphenyl)ethanone (23.8 g, 126 mmol) in acetic acid (100 mL) was treated with N-iodosuccinimide (34.1 g, 151 mmol) and stirred at 70° C. for 2 hr. The reaction mixture was concentrated, diluted with EtOAc and quenched with sat. NaHCO3 solution until the bubbling stopped. The organic layers were separated, washed with water, dried over MgSO4 and stripped to give the desired product which was used in the next step without further purification.

後処理

  1. concentrationThe reaction mixture was concentrated
  2. additiondiluted with EtOAc
  3. customquenched with sat. NaHCO3 solution until the bubbling
  4. customThe organic layers were separated
  5. washwashed with water
  6. dry with materialdried over MgSO4

出典と根拠

ORDレコード
ord-739c2e1325ec4b5cbca0537fbcea6110
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09309251B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート