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HRID 24136作成日:2026年10月24日

Water → 6-Bromo-1,4,4-trimethyl-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/ja/reaction/24136

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物N-(4-Bromophenyl)-N-methyl-3-methyl-2-butenamideHCID 22568913—
溶媒Methylenechloride HexaneHCID 21226440—
生成物6-Bromo-1,4,4-trimethyl-3,4-dihydroquinolin-2(1H)-oneHCID 2256900326.4%

反応手順

N-(4-bromophenyl)-N-methyl-3-methyl-2-butenamide (Intermediate 54, 6.42 g, 24 mmol) was heated to 130° C. and aluminum chloride (5 g, 37.4 mmol) was added in portions over 0.5 h. The reaction mixture was stirred for 1 hour at the same temperature and then cooled to room temperature. Ice was added cautiously to the solid, followed by ˜200 mL of iced water. The reaction mixture was then extracted with ether (×2) and dichloromethane (×1) and the combined organic phase was dried over anhydrous magnesium sulfate and evaporated in vacuo to yield a brown solid. The solid was treated with hexane-dichloromethane and filtered to afford 1.7 g of product. The mother liquor was evaporated and purified by flash column chromatography on silica gel (230-400 mesh) to afford 2.9 g of the title compound as a solid (total 72%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855512B2
出典データセットuspto-grants-2005_02
ORD IDord-b85b6f9e5d254a01ae011c966d72a4e5
出典メモuspto-grants-2005_02