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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2936생성일: 2026년 10월 23일

Ethanol → 5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-2-thioxo-4-thiazolidinone

https://huagongshe.com/ko/reaction/2936

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물WaterHCID 962—
반응물3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
반응물RhodanineHCID 1201546—
용매Acetic AcidHCID 176—
생성물5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-2-thioxo-4-thiazolidinoneHCID 3071511—

반응 단계

Under a nitrogen atmosphere, 117.2 g of 3,5-di-tert-butyl-4-hydroxybenzaldehyde, 66.6 g of rhodanine, and 143.5 g of fused sodium acetate were heated at reflux in 2500 ml of glacial acetic acid. After heating for 23 hours, the reaction mixture was cooled and poured into a mixture of 1 liter of ethanol and 1 liter of ice with stirring. 500 ml of water were added and, after stirring for 30 minutes, the resulting precipitate was recovered by filtration. The solid was slurried with 500 ml of ethyl acetate and filtered. The precipitate was then dissolved in 3 liters of ethanol, heated to boiling, and water was added until the solution remained cloudy (approximately 450 ml). Upon cooling to room temperature, 99.6 g of the desired title product were recovered by filtration, m.p. approximately 260° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731336
출처 데이터셋uspto-grants-1998_03
ORD IDord-c6e9632cd19641829385bd2d3cca13fe
출처 메모uspto-grants-1998_03