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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238533생성일: 2026년 10월 23일

Hydrochloric Acid → 5-Carboxy-2,1,3-benzoxadiazol-1-ium-1-olate

https://huagongshe.com/ko/reaction/238533

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium ChlorideHCID 5234—
반응물Potassium HydroxideHCID 14797—
반응물Benzoic acid, 4-amino-3-nitro-HCID 74115—
반응물Sodium HypochloriteHCID 23665760—
용매Acetic AcidHCID 176—
용매AcetoneHCID 180—
용매EthanolHCID 702—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물5-Carboxy-2,1,3-benzoxadiazol-1-ium-1-olateHCID 33528188.8%

반응 조건

온도67.5 °C

반응 단계

In a 3 L reactor fitted with mechanical stirring, reflux condenser, thermometer and nitrogen inlet, KOH (72.46 g) was dissolved in ethanol (250 ml) and water (250 ml). 4-Amino-3-nitrobenzoic acid (100 g) was added and the orange suspension was heated to 65-70° C. within 30 minutes. The resulting suspension was stirred at the same temperature for 45 minutes and cooled to 0° C.±5° C. within 30 minutes. A commercially available (13% w/w) solution of sodium hypochlorite (448.93 g) was added drop wise within 1.5 hours at 0° C.±5° C. The reaction mixture was stirred at the same temperature for 2 hours and controlled by TLC (CHCl3 100/acetone 2/acetic acid 1). Water (350 ml) was added within 15 minutes at 0° C.±5° C. to give a fine yellow suspension. The reaction mixture was then acidified with a 6N HCl solution (239 ml) until 0.5<pH<1 was reached. Sodium chloride (58.44 g) was added and the resulting suspension was stirred at 0° C.±5° C. for 1.5 hours under nitrogen. The solid was collected by filtration, washed with 3×400 ml water and dried (40° C., 30 mbars, 12 hours) to yield 83.6 g (88.8% yield) of [2,1,3]-benzoxadiazole-5-carboxylic acid N-oxide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642633B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-29c3d43ac8624ee9a6d512f818c6ba35
출처 메모uspto-grants-2014_02