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HRID 1010404作成日:2026年10月26日

Water → N-Methyl-4-benzyloxy-2-methylaniline

https://huagongshe.com/reaction/1010404

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1H-Benzotriazole-1-methanolHCID 224169—
反応物Sodium borohydrideHCID 4311764—
反応物4-(Benzyloxy)-2-methylanilineHCID 16773053—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N-Methyl-4-benzyloxy-2-methylanilineHCID 2293649862.5%

反応手順

After dissolving 4-benzyloxy-2-methylaniline (6.55 g, 30.72 mmol) in N,N-dimethylformamide (10 ml) and methanol (60 ml), 1H-benzotriazole-1-methanol (4.58 g, 30.72 mmol) was added and the mixture was stirred for 30 minutes at room temperature. N,N-Dimethylformamide (20 ml) was added for complete dissolution of the precipitated crystals, sodium borohydride (2.32 g, 61.44 mmol) was added in small portions at a time at room temperature (internal temperature increase), and the mixture was stirred for 30 minutes. Water was added to the reaction solution, extraction was performed ethyl acetate, the extract was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was adsorbed onto silica gel and purified by silica gel column chromatography (hexane-ethyl acetate) to obtain the title compound (4.364 g, 19.20 mmol, 62.49%) as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07973160B2
出典データセットuspto-grants-2011_07
ORD IDord-91f8bdb10a654ebebb34ac3d7bd5ee70
出典メモuspto-grants-2011_07