戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1043887作成日:2026年10月27日

Benzoyl Peroxide → 2-Bromo-5-(methoxymethyl)-1,3-dimethylbenzene

https://huagongshe.com/reaction/1043887

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物2-BromomesityleneHCID 68473—
溶媒Carbon TetrachlorideHCID 5943—
生成物2-Bromo-5-(methoxymethyl)-1,3-dimethylbenzeneHCID 8668632615.4%

反応条件

温度80 °C

反応手順

2-bromomesitylene (5.00 g) was dissolved in carbon tetrachloride (50 mL). NBS (4.45 g) and benzoyl peroxide (182 mg) were added to the solution, and the mixture was stirred at 80° C. for three hours. The reaction mixture was returned to room temperature and filtered. The solid collected by filtration was washed with n-heptane. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (n-heptane). The resulting fraction was concentrated under reduced pressure. The residue was dissolved in THF (120 mL). Sodium methoxide (28% solution in methanol, 9.35 mL) was added to the solution, and the mixture was stirred at 80° C. for four hours. The reaction mixture was returned to room temperature and concentrated under reduced pressure. Water was added to the residue, followed by extraction with DCM. The organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/n-heptane, 0% to 5%). The resulting fraction was concentrated under reduced pressure, and the residue was purified again by NH silica gel column chromatography (n-heptane) to give the title compound (880 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563565B2
出典データセットuspto-grants-2013_10
ORD IDord-9012ecba62c0433ab5a891e812fdb66d
出典メモuspto-grants-2013_10