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HRID 18179作成日:2026年10月26日

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

https://huagongshe.com/reaction/18179

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物PhenolHCID 996—
反応物Potassium IodideHCID 4875—
反応物Ammonium HydroxideHCID 14923—
反応物2-Bromo-4-methylphenolHCID 23109—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物2-Bromo-6-iodo-4-methylphenolHCID 59344907—

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741326B2
出典データセットuspto-grants-2010_06
ORD IDord-46f8c0218ccc42b981649fe9bb0f79e4
出典メモuspto-grants-2010_06