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HRID 381041作成日:2026年10月25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/381041

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 with 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US06303785B1
出典データセットuspto-grants-2001_10
ORD IDord-2d552d7ab3b8473a9427396d735d6537
出典メモuspto-grants-2001_10