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HRID 278666作成日:2026年10月26日

3-Methyl-but-2-enoic acid 4-bromo-phenyl ester → 2H-1-Benzopyran-2-one, 6-bromo-3,4-dihydro-4,4-dimethyl-

https://huagongshe.com/reaction/278666

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-but-2-enoic acid 4-bromo-phenyl esterHCID 733797—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒DichloromethaneHCID 6344—
生成物2H-1-Benzopyran-2-one, 6-bromo-3,4-dihydro-4,4-dimethyl-HCID 2256892359.7%

反応手順

A solution of 3-methyl-but-2-enoic acid 4-bromo-phenyl ester (7 g, 27.6 mmol) in anhydrous dichloromethane (200 mL) was cooled (ice bath) and treated with aluminum chloride (6.6 g, 49.6 mmol) and the reaction mixture was stirred overnight at ambient temperature. The reaction mixture was quenched with saturated aqueous sodium bicarbonate solution and extracted with diethyl ether (×2). The combined organic extract was washed woth brine (×1), dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford an oil which was purified by flash column chromatography over silica gel (230-400 mesh) using 2.5% ethyl acetate in hexane as the eluent to afford the title compound (4.2 g, 57%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06359135B1
出典データセットuspto-grants-2002_03
ORD IDord-ade3ff693d674767b0fd497df83bdae6
出典メモuspto-grants-2002_03