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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1010409생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1010409

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 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07973160B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-297515d9fc1b4a9d9d7c0295af7fbe67
출처 메모uspto-grants-2011_07