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HRID 2936作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物WaterHCID 962—
反応物3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
反応物RhodanineHCID 1201546—
溶媒Acetic AcidHCID 176—
生成物5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-2-thioxo-4-thiazolidinoneHCID 3071511—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731336
出典データセットuspto-grants-1998_03
ORD IDord-c6e9632cd19641829385bd2d3cca13fe
出典メモuspto-grants-1998_03