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HRID 26083作成日:2026年10月26日

Benzyl Bromide → 2-(Benzyloxy)-1-bromo-4-(2-methyloctan-2-YL)benzene

https://huagongshe.com/reaction/26083

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium hydrideHCID 82127—
反応物2-Bromo-5-(2-methyloctan-2-YL)phenolHCID 12788187—
溶媒DimethylformamideHCID 6228—
生成物2-(Benzyloxy)-1-bromo-4-(2-methyloctan-2-YL)benzeneHCID 12882164—

反応手順

To a -18° C. slurry of 23.0 g. (0.575 mole) of potassium hydride in 400 ml. of N,N-dimethylformamide is added over a 45 minute period a solution of 150 g. (0.5 mole) of 2-(4-bromo-3-hydroxyphenyl)-2-methyloctane in 400 ml. of N,N-dimethylformamide (reaction temperature ≤ -15° C.). The reaction mixture is stirred 15 minutes longer after which a solution of 98.3 g. (0.575 mole) of benzyl bromide in 200 ml. of N,N-dimethylformamide is added. The mixture is then warmed to room temperature and stirred 30 minutes longer. It is quenched by addition to 6 liters of ice water. The quenched mixture is extracted six times with 500 ml. of ether. The combined extract is washed twice with one liter portions of water and once with one liter of saturated sodium chloride, dried over magnesium sulfate and evaporated to a quantitative yield of the title product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04147872
出典データセットuspto-grants-1979_04
ORD IDord-b9ccb1c6746043d695dfe0015179ddd7
出典メモuspto-grants-1979_04