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HRID 1028102作成日:2026年10月27日

Pyridine → N-(3-bromo-5-nitrophenyl)acetamide

https://huagongshe.com/reaction/1028102

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Acetyl chlorideHCID 6367—
反応物ar-Bromo-ar-nitrobenzenamineHCID 44535—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-(3-bromo-5-nitrophenyl)acetamideHCID 10658908—

反応条件

温度0 °C

反応手順

3-Bromo-5-nitroaniline (6.45 g, 29.7 mmol) was dissolved in dichloromethane (149 mL) and pyridine (2.88 mL, 35.7 mmol). The solution was cooled to 0° C. and then, acetyl chloride (2.325 mL, 32.7 mmol) was added dropwise. The reaction mixture was stirred at 0° C. for 1 hour. The reaction was diluted with water and dichloromethane and the organic phase was dried over sodium sulfate and was concentrated to dryness. N-(3-bromo-5-nitrophenyl)acetamide was isolated as a beige powder (7.86 g, 30 mmol, 100%) and was of sufficient purity to carry forward without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08735417B2
出典データセットuspto-grants-2014_05
ORD IDord-70ec7c4f20d74ae5b7511b8de2beb47a
出典メモuspto-grants-2014_05