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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2282782생성일: 2026년 10월 26일

Sulfanilic acid → 4-((3,5-Difluoro-4-hydroxyphenyl)diazenyl)benzenesulfonic acid

https://huagongshe.com/reaction/2282782

반응식

참여 물질

역할이름HCID투입량
반응물Sulfanilic acidHCID 8479—
반응물Potassium HydroxideHCID 14797—
반응물2,6-DifluorophenolHCID 94392—
반응물Sodium NitriteHCID 23668193—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물4-((3,5-Difluoro-4-hydroxyphenyl)diazenyl)benzenesulfonic acidHCID 13573744979%

반응 단계

Sulfanilic acid (0.767 g, 4.43 mmol) was dissolved in hot mixture of 20 mL of water and 10 mL of conc. HCl. The solution was cooled in ice/NaCl bath to 0° C. giving a suspension of HCl salt. The solution of sodium nitrite (0.367 g, 5.32 mmol in 5 mL of water) was added dropwise to the suspension of ammonium salt, maintaining the temperature below +5° C. All solid dissolved and the resulting solution was stirred for 20 min. After that white precipitate formed again and the resulting suspension was added dropwise to the mixture of 2,6-difluorophenol (0.576 g, 4.43 mmol) in 10 mL of dioxane and KOH (10 g) in 15 mL of water, cooled in ice/water bath. The reaction mixture was stirred for 30 min in ice/water bath and then extracted with ethyl acetate (3×30 mL). The aqueous solution was acidified with 10% HCl to pH 2-3 and the formed yellow precipitate was collected, washed with water and dried in vacuum to give phenol 2 as a yellow powder (1.1 g, 79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09140706B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-dea014818bc0461e92a40d7d87eca443
출처 메모uspto-grants-2015_09