Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | 3,3-Dimethyl-2-oxobutanenitrile | HCID 94527 | — |
| Edukt | Thiocarbohydrazide | HCID 2724189 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Produkt | HCID 178441961 | HCID 178441961 | 97,1% |
Reaktionsschritte
First 25.6 g (0.25 mol) of acetic anhydride and then 27.8 g (0.25 mol) of pivaloyl cyanide were introduced, in each case at room temperature, into 49.0 g (0.5 mol) of concentrated sulphuric acid, which had been initially introduced into the reaction vessel. After subsequently stirring this reaction mixture for 0.5 hour, it was stirred into a solution of 26.6 g (0.25 mol) of thiocarbohydrazide in 300 ml of 1 N HCl at 20°-30° C. When the addition had ended, the mixture was subsequently stirred at 50°-55° C. for a further 1.5 hours; after cooling, the reaction product which had precipitated was filtered off, washed with 200 ml of water and dried. 48.6 g (97% of theory) of 4-amino-6-tert.-butyl-3-mercapto-1,2,4-triazin-5(4H)-one (V) were obtained as colorless crystals of melting point 212°-214° C.; content according to a determination by gas chromatography >99 %. No further purification operations were necessary for subsequent reactions.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04328340 |
|---|
| Quelldatensatz | uspto-grants-1982_05 |
|---|
| ORD ID | ord-c49fc2677e874fb7b13f2a099cde28b2 |
|---|
| Quellennotiz | uspto-grants-1982_05 |
|---|