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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1291939생성일: 2026년 10월 23일

Water → 2,5-Bis[4-(3,4-dimethyl-5-isoxazolyl)sulfamoylanilino]terephthalic acid

https://huagongshe.com/ko/reaction/1291939

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sulfuric AcidHCID 1118—
반응물SulfisoxazoleHCID 5344—
반응물Potassium HydroxideHCID 14797—
반응물Sodium 3-nitrobenzenesulfonateHCID 31389—
반응물Dimethylsuccinyl succinateHCID 131720661—
용매MethanolHCID 887—
생성물2,5-Bis[4-(3,4-dimethyl-5-isoxazolyl)sulfamoylanilino]terephthalic acidHCID 1891370870.4%

반응 조건

온도50 °C

반응 단계

To 150 g of methanol was added with stirring 20 g (87.6 mmol) of dimethylsuccinyl succinate, 53.9 g (201.6 mmol) of 4-amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulfonamide (Aldrich Chemical Co.), and 0.7 g of concentrated sulfuric acid. The reaction mixture was heated slowly to 95° to 97° C. and maintained at that temperature for five hours. After the reaction mixture was cooled to 50° C., 26 g of sodium 3-nitrobenzenesulfonate, 2 g of water, and 75 g of 45% aqueous potassium hydroxide were slowly added with stirring. The resultant mixture was then slowly heated to 90° C and maintained at that temperature for four hours. The reaction mixture was cooled to room temperature and added to 500 ml of water. Concentrated sulfuric acid was slowly added to produce a solid that was collected by filtration and washed with water. The wet presscake was dried in an oven to give 43 g (70.4% of theory) of 2,5-bis[4-(3,4-dimethyl-5-isoxazolyl)sulfamoylanilino]terephthalic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05755873
출처 데이터셋uspto-grants-1998_05
ORD IDord-5bf4fed710744353ab0975c0e0ea28b7
출처 메모uspto-grants-1998_05