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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30866생성일: 2026년 10월 24일

Formic Acid → N-(2-fluoro-4-iodophenyl)formamide

https://huagongshe.com/ko/reaction/30866

반응식

참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물Acetic AnhydrideHCID 7918—
반응물2-Fluoro-4-iodoanilineHCID 185694—
용매Hydrochloric AcidHCID 313—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물N-(2-fluoro-4-iodophenyl)formamideHCID 2354934197.1%

반응 단계

To a cooled solution (0° C.) of 4-iodo-2 fluoroaniline (3.05 g, 12.9 mmol) in tetrahydrofuran (15 mL) and toluene (15 mL), was slowly added a mixture of acetic anhydride (1.39 mL, 14.7 mmol) and formic acid (0.83 mL, 22.0 mmol). The reaction mixture was stirred at rt overnight, then diluted with ethyl acetate (100 mL) and 1N aqueous HCl (100 mL). The layers were separated, and the organic layer was washed with water and saturated sodium carbonate solution, and dried over sodium sulfate. The solvent was removed under reduced pressure to afford 2-fluoro-4-iodophenylformamide as an off-white solid (3.32 g, 97%). GC-MS ret. time 2.27 min, m/z 265 (M+); 1H NMR (300 MHz, CDCl3) δ: 7.37-7.51 (m, 3H), 8.13 (t, 1H), 8.46 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423156B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-22b4e1dc687b469fadcc66f83c4a3b41
출처 메모uspto-grants-2008_09