Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbamate | HCID 276 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2,4-Dichloro-6-(dimethylamino)-1,3,5-triazine | HCID 16985 | — |
| Edukt | Ethyl ethoxythiocarbonylcarbamate | HCID 3457746 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | 2-Chloro-4-ethoxy-6-dimethylamino-1,3,5-triazine | HCID 23338142 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 178467450 | HCID 178467450 | — |
Reaktionsschritte
Ethyl ethoxythiocarbonylcarbamate (1 molar proportion) was added to a stirred solution of potassium carbonate in water (10 ml. per gram of carbamate). After 15 minutes stirring, the solution was filtered and dimethyl sulphate added dropwise to the filtrate with vigorous stirring over 45 minutes. The mixture was then stirred for 1 hour and extracted with light petroleum. The extracts were dried and cooled to -40° C., when the carbamate separated. Recrystallised from petroleum, the carbamate had a melting point of 38°-39° C. (b) N,N-Dimethylguanidine hydrochloride (3.23 g; 0.026 mol.) was added to a solution of sodium (0.61 g; 0.026 mol.) in anhydrous ethanol (50 ml.) and the mixture was heated under reflux for 30 minutes. The carbamate prepared in (a) above (5.0 g., 0.026 mol.) was then added and the mixture heated under reflux for 22 hours. The ethanol was removed, water (75 ml.) added, and the pH of the solution adjusted to 6 to 7 with acetic acid. The product was collected, washed with water, and recrystallised from ethanol to give 4-dimethylamino-6-ethoxy-1,3,5-triazin-2-one.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04082536 |
|---|
| Quelldatensatz | uspto-grants-1978_04 |
|---|
| ORD ID | ord-67e8774646044b929977253ff5a2ce63 |
|---|
| Quellennotiz | uspto-grants-1978_04 |
|---|