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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275099생성일: 2026년 10월 25일

Ethanol → 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine

https://huagongshe.com/reaction/275099

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Potassium HydroxideHCID 14797—
반응물methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamateHCID 15766845—
용매WaterHCID 962—
생성물4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 1527938998.3%

반응 단계

4N potassium hydroxide aqueous solution (4.75 liters) was added to an ethanol solution (3 liters) of methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate (2.25 kg, 7.85 mol) and the mixture was heated under reflux for 5 hours. After reaction, the reaction liquid was cooled to room temperature, water (5 liters) was added thereto, and this was extracted with toluene (5 liters×2). The organic layer was washed with water and then dried over anhydrous magnesium sulfate. The drying agent was taken out by filtration, and the solvent was removed by distillation under reduced pressure to obtain an oily product of 2-fluoro-4-chloro-5-cyclopentyloxyaniline (1.75 kg, 7.62 mol). Yield: 98.3%. Spectral data and other data of the product are those as shown in Example 21.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05391807
출처 데이터셋uspto-grants-1995_02
ORD IDord-26a7ca6f0d9d415bb97985d3cdfe3487
출처 메모uspto-grants-1995_02