HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34424Erstellt: 24. Oktober 2026
Water → 2-(2-Pinanylthio)-5-(t-butylthio)-1,3,4-thiadiazole
https://huagongshe.com/de/reaction/34424
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | tert-Butanol | HCID 6386 | — |
| Edukt | (+-)-alpha-Pinene | HCID 6654 | — |
| Edukt | HCID 178418558 | HCID 178418558 | — |
| Katalysator | Sulfuric Acid | HCID 1118 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | 2-(2-Pinanylthio)-5-(t-butylthio)-1,3,4-thiadiazole | HCID 20129852 | — |
Reaktionsschritte
2,5-Dimercapto-1,3,4-thiadiazole (35 g, 0.23 mol) and alpha-pinene (35 g, 0.26 mol) were charged to a reaction vessel and heated cautiously to 140° C. (exothermic reaction). The reaction was maintained at 135°-155° C. for 15 min. The reaction was fitted with a Dean Stark trap filled with xylene. Xylene (15 ml) was charged to the reaction. The reaction was fitted with an addition funnel containing t-butanol (25 g, 0.34 mol). The alcohol was added slowly with the reaction refluxing. Sulfuric acid (3 drops) was added to accelerate the water removal. The reaction product was isolated after approximately 5 ml (about 0.25 mol) of water were collected. Solvent was stripped by rotary evaporation. The product was mixed with calcium hydroxide (1 g), hexane (about 100 ml), and sufficient acetone (about 50 ml) to maintain one liquid layer. The product was filtered using a filter aid and the solvent removed by rotary evaporation. This afforded the final product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04761482 |
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| Quelldatensatz | uspto-grants-1988_08 |
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| ORD ID | ord-ba1ce414a207408996063908143efced |
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| Quellennotiz | uspto-grants-1988_08 |
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