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Iodine → 4-Bromo-2-ethoxy-1-iodobenzene

HRID 735663
ノート
印刷プレビュー

反応式

HRID 735663 の反応式
[Br:1][C:2]1[CH:8]=[CH:7][C:5](N)=[C:4]([O:9][CH2:10][CH3:11])[CH:3]=1.[I:12]I>C(#N)C>[Br:1][C:2]1[CH:8]=[CH:7][C:5]([I:12])=[C:4]([O:9][CH2:10][CH3:11])[CH:3]=1
参加物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 807IodineHCID 155555024-Bromo-2-ethoxyaniline

生成物 1

HCID 509981894-Bromo-2-ethoxy-1-iodobenzene収率 509.8%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒2 回

実験手順

To a solution of 62B (2.5 g, 1.2 mmol) in acetonitrile (30 mL) at 0° C. was added dropwise a solution of iodine (6 g, 2.4 mmol), and t-BuONO (1.44 g, 1.4 mmol) in acetonitrile (100 mL) over 30 min and stirred 1.5 h. The mixture was quenched with aqueous Na2SO3 while maintaining the temperature <10° C. After stirring 1 h the mixture was extracted with hexane (3×100 mL). The combined organics were dried (MgSO4) before concentrating in vacuo and the residue was purified by flash chromatography (0-5% EtOAc/Hexane) to afford 62C (2 g, 53%) as an oil. 1H NMR (400 MHz, CDCl3) δ ppm 1.47 (t, J=7.03 Hz, 4 H) 4.06 (q, J=7.03 Hz, 2 H) 6.83 (dd, J=8.35, 1.76 Hz, 1 H) 6.90 (d, J=2.20 Hz, 1 H) 7.59 (d, J=8.35 Hz, 1 H).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThe mixture was quenched with aqueous Na2SO3
  2. temperaturewhile maintaining the temperature <10° C
  3. stirringAfter stirring 1 h the mixture
  4. extractionwas extracted with hexane (3×100 mL)
  5. dry with materialThe combined organics were dried (MgSO4)
  6. concentrationbefore concentrating in vacuo
  7. customthe residue was purified by flash chromatography (0-5% EtOAc/Hexane)

出典と根拠

ORDレコード
ord-e3eed22c3ac1407290d5117a6b8e7c99
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07592331B2

反応ノート

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