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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12440생성일: 2026년 10월 23일

Acetic Acid → 1-(2,4-Dihydroxy-phenyl)-5-(4-fluoro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid

https://huagongshe.com/ko/reaction/12440

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물WaterHCID 962—
반응물Acetic AnhydrideHCID 7918—
반응물1-(5-Chloro-2,4-dimethoxy-phenyl)-5-(4-fluoro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acidHCID 58731018—
용매Hydrogen iodideHCID 24841—
생성물1-(2,4-Dihydroxy-phenyl)-5-(4-fluoro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acidHCID 11483871—

반응 단계

1-(5-Chloro-2,4-dimethoxy-phenyl)-5-(4-fluoro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid (0.29 g, 0.77 mmol) was refluxed in a mixture of hydroiodic acid (5 mL), acetic acid (1 mL) and acetic anhydride (0.5 mL) for 16 hours. When cooled, water (20 mL) was added and the aqueous layer was extracted with EtOAc (2×15 mL). The combined organic layers were washed with saturated sodium thiosulphate solution (2×15 mL) and brine (20 mL), dried with NaSO4 and filtered. After evaporation of the solvent, light brown solids were obtained (0.15 g, 62%). The compound was used in the next synthetic step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728016B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-4325811208714cde96d7855dd97c1686
출처 메모uspto-grants-2010_06