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HRID 1028102생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1028102

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Acetyl chlorideHCID 6367—
반응물ar-Bromo-ar-nitrobenzenamineHCID 44535—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-(3-bromo-5-nitrophenyl)acetamideHCID 10658908—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08735417B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-70ec7c4f20d74ae5b7511b8de2beb47a
출처 메모uspto-grants-2014_05