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HRID 853541作成日:2026年10月25日

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

https://huagongshe.com/reaction/853541

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US07253286B2
出典データセットuspto-grants-2007_08
ORD IDord-a498f4e50f3c4177aa2892464d055671
出典メモuspto-grants-2007_08