Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586731Generated: November 1, 2026

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

https://huagongshe.com/reaction/1586731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
Reactant3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
ReactantRhodanineHCID 1201546—
SolventAcetic AcidHCID 176—
Product5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-2-thioxo-4-thiazolidinoneHCID 3071511—

Reaction Steps

Under a nitrogen atmosphere, 117.2 g of 3,5-di-tert-butyl-4-hydrox-ybenzaldehyde, 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05216002
Source datasetuspto-grants-1993_06
ORD IDord-2b7976e9b2634262b4248ad1c55a4b36
Source noteuspto-grants-1993_06