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HRID 273883作成日:2026年10月27日

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

https://huagongshe.com/reaction/273883

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. Water (500 ml) was 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 dissolved in 3 liters of ethanol, heated to boiling, and water was added until the solution remained cloudy (approximately 450 ml of water). Upon cooling to room temperature, 99.6 g of 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US05387690
出典データセットuspto-grants-1995_02
ORD IDord-d5974493f8b34b6ab6ddbe1d4a5f086c
出典メモuspto-grants-1995_02