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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1892499생성일: 2026년 10월 24일

Water → 5-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]vinyl}thiophene-2-carboxylic acid

https://huagongshe.com/ko/reaction/1892499

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물5-Formyl-2-thiophenecarboxylic AcidHCID 818882—
반응물Potassium tert-butoxideHCID 23665647—
반응물[(2-Acetylaminothiazol-4-yl)methyl](triphenyl)phosphonium chlorideHCID 86092822—
용매DimethylformamideHCID 6228—
생성물5-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]vinyl}thiophene-2-carboxylic acidHCID 8665000558.6%

반응 단계

To a solution of {[2-(acetylamino)-1,3-thiazol-4-yl]methyl}(triphenyl)phosphonium chloride (3.771 g, 8.325 mmol) in anhydrous N,N-dimethylformamide (35 ml) was added potassium tert-butoxide (2.515 g, 22.41 mmol) at 0° C., and the mixture was stirred for 15 min. 5-Formylthiophene-2-carboxylic acid (1.000 g, 6.404 mmol) was added by small portions, and the mixture was stirred at 0° C. for 30 min. The mixture was warmed to room temperature, stirred for 2 hr, and poured into iced water (300 ml). After stirring for 30 min, the mixture was washed twice with ethyl acetate. The aqueous layer was cooled to 0° C., and adjusted to pH 3 by dropwise addition of 6M hydrochloric acid. After stirring at 0-5° C. for 2 hr, the precipitated crystals were collected by filtration, washed 3 times with water, and twice with diisopropyl ether and dried under reduced pressure to give 5-{2-[2-(acetylamino)-1,3-thiazol-4-yl]vinyl}thiophene-2-carboxylic acid (1.104 g, 3.751 mmol, yield 58.6%) as a yellow ocher solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08507690B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-e8dd722b52a647b88e8e9a2d0ea64d7b
출처 메모uspto-grants-2013_08