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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542004생성일: 2026년 10월 23일

2-Iodo-4-nitroaniline → 1-Fluoro-2-iodo-4-nitrobenzene

https://huagongshe.com/ko/reaction/542004

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참여 물질

역할이름HCID투입량
반응물2-Iodo-4-nitroanilineHCID 222629—
반응물Nitrilooxonium tetrafluoroborateHCID 11137142—
용매DichloromethaneHCID 6344—
생성물1-Fluoro-2-iodo-4-nitrobenzeneHCID 1053973338%

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온도0 °C

반응 단계

A solution of nitrosonium tetrafluoroborate (24 g, 0.21 mol) in dichloromethane (200 mL) at 0° C. was treated with a solution of 2-iodo-4-nitroaniline (50 g, 0.19 mol) in dichloromethane (350 mL) and stirred at 0° C. for 1 h. The dichloromethane was concentrated to about half volume and the reaction mixture was treated with 1,2-dichlorobenzene (300 mL). The remaining dichloromethane was further concentrated in vacuo. The resultant 1,2-dichlorobenzene suspension was heated at 110° C. for 1 h, cooled to 20° C., and treated with water (200 mL) and dichloromethane (500 mL). The reaction mixture was filtered over celite and the celite was washed with dichloromethane and water. The aqueous layer of the filtrate was separated and extracted with dichloromethane (2×). The combined organic layers were washed with 20% sodium thiosulfate and brine, dried over anhydrous sodium sulfate, and filtered. The dichloromethane was removed under standard conditions while the 1,2-dichlorobenzene was removed via vacuum distillation to give a crude dark oil. This material was purified by distillation to give the desired product (19 g, 38%) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871753B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-837a55d8d67b4df4970587f1e6089a35
출처 메모uspto-grants-2014_10