돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1034111생성일: 2026년 10월 25일

Potassium Cyanide → 2-Fluoro-4-iodobenzonitrile

https://huagongshe.com/reaction/1034111

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CyanideHCID 9032—
반응물Sodium HydroxideHCID 14798—
반응물2-Fluoro-4-iodoanilineHCID 185694—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium NitriteHCID 23668193—
촉매Copper sulfate pentahydrateHCID 24463—
용매Acetic AcidHCID 176—
용매BenzeneHCID 241—
용매WaterHCID 962—
용매Sulfuric AcidHCID 1118—
생성물2-Fluoro-4-iodobenzonitrileHCID 277451829.5%

반응 단계

27 g of sodium nitrite was dissolved in 205 ml of sulfuric acid and cooled to 10° C. or less, and then 238 ml of acetic acid was added. At 20° to 25° C., 65 g of 2-fluoro-4-iodoaniline was added to the solution, and then the solution was agitated for one hour. A second solution was made by dissolving 82.5 g of copper sulfate pentahydrate in 20.5 ml of water, to which was added 140 g of ice, and this solution was added to the first. A third solution containing 88 g of potassium cyanide dissolved in 207 ml of water, 500 g of sodium bicarbonate, and 206 ml of benzene was added to the first solution, and a diazonium salt sulfuric acid solution was added therein. After agitation at room temperature for 3 hours, a sodium hydroxide aqueous solution was added to dissolve the crystals. After being extracted with chloroform, the crystals were washed three times alternating with a 10% sodium hydroxide solution and water. After distillation of the chloroform, the residue was extracted with hexane, and the hexane was distilled off. This residue was subjected to vacuum distillation (95° to 110° C./15 mmHg), and further recrystallized to obtain 20 g of 1-cyano-2-fluoro-4-iodobenzene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05314640
출처 데이터셋uspto-grants-1994_05
ORD IDord-6c4afcb0019747d1ab02f0eeafc1bcd1
출처 메모uspto-grants-1994_05