HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethanol → [(1,3,4-Thiadiazol-2,5-diyl)dithio]-bis(2,2'-succinic acid)
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Bromosuccinic acid | HCID 73557 | — |
| Edukt | HCID 178418558 | HCID 178418558 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | [(1,3,4-Thiadiazol-2,5-diyl)dithio]-bis(2,2'-succinic acid) | HCID 14646898 | — |
Reaktionsschritte
About 68 g. of a solution of 39.6 g. (0.6 mole) of KOH (85%) in 200 ml. of abs. ethanol is added to a stirred slurry of 15.0 g. (0.1 mole) of 2,5-dimercapto-1,3,4-thiadiazole in 80 ml. of abs. ethanol, at 10°-15° C. The resultant mixture is stirred at 10°-15° C. for half hour thereafter, a clear solution of 39.4 g. (0.2 mole) of bromosuccinic acid in 70 ml. of abs. ethanol is added dropwise over a period of 15 minutes at 10°-15° C. followed by the gradual addition of the remainder of the KOH solution at the same temperature range over a period of 15 minutes. After adding 100 ml. of abs. ethanol, the reaction mixture is stirred in the cooling bath for more than one hour, then overnight in water bath at ambient temperature.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04990652 |
| Quelldatensatz | uspto-grants-1991_02 |
| ORD ID | ord-4d86d0665c834e09a920b9983f2b6ec4 |
| Quellennotiz | uspto-grants-1991_02 |