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HRID 275099作成日:2026年10月26日

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

https://huagongshe.com/reaction/275099

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Potassium HydroxideHCID 14797—
反応物methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamateHCID 15766845—
溶媒WaterHCID 962—
生成物4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 1527938998.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05391807
出典データセットuspto-grants-1995_02
ORD IDord-26a7ca6f0d9d415bb97985d3cdfe3487
出典メモuspto-grants-1995_02