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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388022생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/388022

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium borohydrideHCID 4311764—
반응물Tetrahydrofuran ethyl acetateHCID 21939870—
반응물N-{1-(1H-Benzotriazolyl)methyl}-4-benzyloxy-2-fluoroanilineHCID 22936313—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물N-Methyl-4-benzyloxy-2-fluoroanilineHCID 2293665864.9%

반응 단계

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 saline 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372981B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-1ce321c63ebf4659ab4778e9a44e8a33
출처 메모uspto-grants-2013_02