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HRID 59636作成日:2026年10月23日

2-Aminophenol → 4-Fluoro-N-(2-hydroxyphenyl)benzamide

https://huagongshe.com/ja/reaction/59636

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminophenolHCID 5801—
反応物2-MethyltetrahydrofuranHCID 7301—
反応物4-Fluorobenzoyl chlorideHCID 67879—
反応物DiosgeninHCID 99474—
反応物Sodium BicarbonateHCID 516892—
溶媒WaterHCID 962—
生成物4-Fluoro-N-(2-hydroxyphenyl)benzamideHCID 579383—

反応条件

温度60 °C

反応手順

To a 500 ml 4 necked round bottom flask equipped with a thermometer, a mechanic stirrer, a drop funnel, a nitrogen in-let, was added sodium bicarbonate (29.6 g, 0.354 mol, 1.1 eq), 2-aminophenol (34.88 g, 0.32 mol, 1 eq) and 2-Methyl THF (250 ml). The temperature of the mixture was controlled under 20° C. by ice-bath. Under vigorously stirring, 4-fluorobenzoyl chloride (50.72 g, 0.32 mol, 1 eq) was added drop wise within 10 min. Then the reaction was allowed to be stirred for another 1.5 hrs. When HPLC data showed that less than 0.3% of 2-aminophenol remained, 100 ml of water and 50 ml of 2-methyl tetrahydrofuran was added to quench the reaction and then the mixture was heated to 60° C. with stirring. The mixture was partitioned into two phases and the organic phase was washed with 100 ml of 1N H2SO4 and subsequently with 100 ml of water. Then the solvent was evaporated to almost dryness with stirring.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440935B2
出典データセットuspto-grants-2016_09
ORD IDord-184b04ec7f5642aabf0759c1f6f1a299
出典メモuspto-grants-2016_09