HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 839950Erstellt: 24. Oktober 2026
Hydrochloric Acid → 5-(Trifluoromethyl)-1,3,4-thiadiazole-2(3H)-thione
https://huagongshe.com/de/reaction/839950
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Thiourea | HCID 2723790 | — |
| Edukt | 2-Bromo-5-(trifluoromethyl)-1,3,4-thiadiazole | HCID 12874685 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 5-(Trifluoromethyl)-1,3,4-thiadiazole-2(3H)-thione | HCID 178506284 | 59,1% |
Reaktionsschritte
699 g (3 moles) of 2-bromo-5-trifluoromethyl-1,3,4-thiadiazole and 248 g (3.3 moles) of thiourea in a mixture of 600 ml of ethanol and 75 ml of water were heated for 2 hours under reflux. A solution of 223 g of potassium hydroxide in 2 liters of water was rapidly added dropwise to the reaction solution while it was still hot, and the mixture was once more heated under reflux, for 5 minutes. The cooled solution was adjusted to pH 5 with dilute hydrochloric acid and extracted repeatedly with methylene chloride. After drying and concentrating, the residue was recrystallized from a litte petroleum ether. The mother liquor yielded further product. 330 g (59% of theory) of 2-mercapto-5-trifluoromethyl-1,3,4-thiadiazole of melting point 73° C were obtained. ##STR85##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04097669 |
|---|
| Quelldatensatz | uspto-grants-1978_06 |
|---|
| ORD ID | ord-6c9548cdd0e74e8c940976af7dbedd69 |
|---|
| Quellennotiz | uspto-grants-1978_06 |
|---|