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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388023생성일: 2026년 10월 25일

Water → N-(4-Benzyloxy-2-fluorophenyl)-N'-(4-fluorophenyl)-N-methylurea

https://huagongshe.com/reaction/388023

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물4-Fluorophenyl isocyanateHCID 70955—
반응물N-Methyl-4-benzyloxy-2-fluoroanilineHCID 22936658—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(4-Benzyloxy-2-fluorophenyl)-N'-(4-fluorophenyl)-N-methylureaHCID 2293649426.7%

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온도95 °C

반응 단계

N-Methyl-4-benzyloxy-2-fluoroaniline (250 mg, 1.0805 mmol) was dissolved in N,N-dimethylformamide (5.0 ml), and then sodium hydride (65 mg, 1.6207 mmol, 60% in oil) was added and the mixture was stirred at 95° C. for 45 minutes under a nitrogen atmosphere. After adding 4-fluorophenyl isocyanate (0.14 ml, 1.1836 mmol), the mixture was stirred at 85° C. for 45 minutes under a nitrogen atmosphere. There was further added 4-fluorophenyl isocyanate (0.14 ml, 0.5094 mmol), and the mixture was stirred at 85° C. for 30 minutes under a nitrogen atmosphere. After cooling to room temperature, water was added to the reaction solution, extraction was performed with ethyl acetate, 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 NH silica gel and purified by NH silica gel column chromatography (hexane-ethyl acetate system) to obtain the title compound (0.105 g, 0.2881 mmol, 21.67%) as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372981B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-23cec06d6e4548f289965501a4c4ca28
출처 메모uspto-grants-2013_02