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HRID 323684作成日:2026年10月25日

2-Ethyl-6-methylphenol → 4-Bromo-2-ethyl-6-methylphenol

https://huagongshe.com/reaction/323684

反応式

関与物質

役割名称HCID仕込み量
反応物2-Ethyl-6-methylphenolHCID 519333—
反応物Tetra-n-butylammonium tribromideHCID 23500184—
溶媒ChloroformHCID 6212—
生成物4-Bromo-2-ethyl-6-methylphenolHCID 22006838182.7%

反応条件

温度0 °C

反応手順

Then, 16 g of 2-ethyl-6-methylphenol was dissolved in 200 ml of chloroform, which was stirred at 0° C., and 56.6 g of tetrabutylammonium tribromide was added in small portions to this solution. After stirring at room temperature for 1 hour, the solvent was distilled out under reduced pressure. The residue was dissolved in 300 ml of diethyl ether, successively washed with 10% hydrochloric acid and water, dried over anhydrous magnesium sulfate, and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 23 g of 4-bromo-2- ethyl-6-methylphenol (92% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06214835B1
出典データセットuspto-grants-2001_04
ORD IDord-f0caecc358eb4b89a5c7f398cc8089aa
出典メモuspto-grants-2001_04