Iodine → 2-Bromo-6-iodo-4-methylphenol

HRID 18179

反応式

HRID 18179 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[OH:9].[OH-].[NH4+].[I-:12].[K+].II.C1(O)C=CC=CC=1>CO.O>[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([I:12])[C:3]=1[OH:9]

参加物

8

反応条件

温度
60 °C

実験手順

2-Bromo-4-methylphenol (10.11 gm, 54.05 mmol) was mixed with concentrated ammonium hydroxide (50 ml) and methanol (20 ml). Potassium iodide (17.94 g, 108 mmol), iodine (13.72 g, 54.05 mmol) and water (60 ml) were mixed to give a dark brown solution which was added in portions to the phenol solution. Additional methanol (200 ml) was added in portions as precipitating product made the mixture too viscous to stir. When all the iodine solution had been added the mixture was heated to 60° C. till the brown color faded. The mixture was cooled, filtered and the solid rinsed three times with water. The solid was dissolved in dichloromethane, dried over magnesium sulfate, filtered and stripped to give 2-Bromo-4-methyl-6-iodophenol as an oil that crystallized on standing. The filtrate and water rinses were concentrated and extracted twice with ethyl acetate, dried over magnesium sulfate, filtered and stripped to give additional 2-bromo-4-methyl-6-iodophenol for a total of 16.24 g, 96% yield.

後処理

  1. customto give a dark brown solution which
  2. customas precipitating product
  3. additionWhen all the iodine solution had been added the mixture
  4. temperatureThe mixture was cooled
  5. filtrationfiltered
  6. washthe solid rinsed three times with water
  7. dissolutionThe solid was dissolved in dichloromethane
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered

出典と根拠

ORDレコード
ord-46f8c0218ccc42b981649fe9bb0f79e4
出典データセット
uspto-grants-2010_06
特許番号
US07741326B2

関連ノート

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