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HRID 344732作成日:2026年10月26日

4-Methoxyphenol → 2-(4-Methoxyphenoxy)-2-methylpropanal

https://huagongshe.com/reaction/344732

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethoxyphenolHCID 9015—
反応物Sodium HydroxideHCID 14798—
反応物1,1-Dichloro-2-hydroxy-2-methylpropaneHCID 10964627—
触媒Hexadecyltrimethylammonium BromideHCID 5974—
溶媒Diethyl EtherHCID 3283—
生成物2-(4-Methoxyphenoxy)-2-methylpropanalHCID 15192047—

反応手順

A solution of 4-methoxyphenol, (21.72 g, 0.175 mol), in aqueous sodium hydroxide solution, (5.8M, 30 ml), was treated with cetyltrimethyl ammonium bromide, (0.255 g, 0.7 mmol), followed by a solution of 1,1-dichloro-2-hydroxy-2-methylpropane, (5.01 g, 35 mmol), in ether, (70 ml). The mixture was stirred under an argon atmosphere for 18 hours then diluted with ether, (100 ml), and extracted with aqueous sodium hydroxide solution, (2M, 4×50 ml), to remove unreacted phenol. The combined aqueous extracts were extracted with ether, (100 ml), and the organic phase was washed with aqueous sodium hydroxide solution, (2M, 50 ml), and water, (100 ml). The combined organic extracts were dried, (MgSO4), concentrated and purified by flash column chromatography, eluting with ethyl acetate/hexane, (10%, v/v), to give 2-(4-methoxyphenoxy)-2-methylpropanal, (3.61 g), as an oil; NMR: 1.36(6H,s), 3.76(3H,s), 6.7-6.9(4 H,m) and 9.85(1H,s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05053415
出典データセットuspto-grants-1991_10
ORD IDord-90a5560f32674f5fbefba900c71ff540
出典メモuspto-grants-1991_10