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HRID 1010409作成日:2026年10月26日

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

https://huagongshe.com/reaction/1010409

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium borohydrideHCID 4311764—
反応物Tetrahydrofuran ethyl acetateHCID 21939870—
反応物N-{1-(1H-Benzotriazolyl)methyl}-4-benzyloxy-2-fluoroanilineHCID 22936313—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
生成物N-Methyl-4-benzyloxy-2-fluoroanilineHCID 2293665864.9%

反応手順

After dissolving N-{1-(1H-benzotriazolyl)methyl}-4-benzyloxy-2-fluoroaniline (14.13 g, 40.56 mmol) in N,N-dimethylformamide (200 ml), methanol (150 ml) and ethanol (50 ml), there was added sodium borohydride (3.06 g, 81.12 mmol) and the mixture was stirred for 2.5 hours at room temperature. There was further added sodium borohydride (0.78 g, 20.28 mmol), and the mixture was stirred for 13.5 hours at room temperature. Water was added to the reaction solution, extraction was performed with ethyl acetate-tetrahydrofuran, 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 system) to obtain the title compound (5.98 g, 26.31 mmol, 64.87%) as light yellow crystals.

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-297515d9fc1b4a9d9d7c0295af7fbe67
出典メモuspto-grants-2011_07