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HRID 853547作成日:2026年10月25日

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

https://huagongshe.com/reaction/853547

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US07253286B2
出典データセットuspto-grants-2007_08
ORD IDord-29db2766656c438a89f5b3a2b6d06772
出典メモuspto-grants-2007_08