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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 365953생성일: 2026년 10월 26일

Hydrochloric Acid → 2-Carboxy-5-nitrobenzenesulfonic acid potassium salt

https://huagongshe.com/reaction/365953

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Methyl-5-nitrobenzenesulfonic acidHCID 8458—
반응물Potassium HydroxideHCID 14797—
반응물ChlorineHCID 24526—
반응물Sodium HypochloriteHCID 23665760—
생성물2-Carboxy-5-nitrobenzenesulfonic acid potassium saltHCID 45358875—

반응 조건

온도65 °C

반응 단계

27.2 g of 79.8% strength 2-methyl-5-nitrobenzenesulfonic acid (0.1 mol) were added to a mixture of 10.1 ml of 40% strength aqueous potassium hydroxide (0.1 mol) and 141 ml (0.3 mol) of aqueous sodium hypochlorite. The resulting suspension was heated to 65° C. and, at this temperature, admixed with 23 ml of 40% strength aqueous potassium hydroxide (0.23 mol) at a rate of 0.04 ml/min. After the addition was complete, the mixture was cooled to 0° C. and then admixed with 12.24 g (0.3 mol) of KOH. Over a period of 30 min, 10.64 g (0.15 mol) of chlorine gas were then introduced at this temperature. The temperature was then increased to 65° C., aqueous KOH (40% strength, 9.0 ml, 0.9 mol) was added at 0.04 ml/min and the mixture was subsequently stirred at 65° C. for another 2 hours. After cooling to 50° C., the mixture was acidified dropwise with concentrated hydrochloric acid (37% strength, 18 ml, 0.22 mol) at 50° C. over a period of 1 hour, cooled to 15-20° C. while passing through nitrogen gas, thus removing remaining chlorine gas, and stirred at 15-20° C. for another 2 hours. The product 2-carboxy-5-nitrobenzenesulfonic acid monopotassium salt was obtained, after filtration and drying at 75° C./100 mbar as a white powder; yield: 31 g; 76.5% pure product (83.1 % of theory).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06127572
출처 데이터셋uspto-grants-2000_10
ORD IDord-3e197890e07944bfa3a0f24103777768
출처 메모uspto-grants-2000_10