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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethanol | HCID 702 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 3,5-Di-tert-butyl-4-hydroxybenzaldehyde | HCID 73219 | — |
| Edukt | Rhodanine | HCID 1201546 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-2-thioxo-4-thiazolidinone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05387690 |
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| Quelldatensatz | uspto-grants-1995_02 |
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| ORD ID | ord-d5974493f8b34b6ab6ddbe1d4a5f086c |
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| Quellennotiz | uspto-grants-1995_02 |
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