戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1433680作成日:2026年10月27日

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

https://huagongshe.com/reaction/1433680

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US07612092B2
出典データセットuspto-grants-2009_11
ORD IDord-23425df8c8ec4f1f93c19d4789828845
出典メモuspto-grants-2009_11