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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273883Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/273883

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktWaterHCID 962—
Edukt3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
EduktRhodanineHCID 1201546—
LösungsmittelAcetic AcidHCID 176—
Produkt5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-2-thioxo-4-thiazolidinoneHCID 3071511—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05387690
Quelldatensatzuspto-grants-1995_02
ORD IDord-d5974493f8b34b6ab6ddbe1d4a5f086c
Quellennotizuspto-grants-1995_02