Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Isopropanol | HCID 3776 | — |
| Edukt | Cyanamide | HCID 9864 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Produkt | HCID 178458952 | HCID 178458952 | 69,8% |
Reaktionsschritte
11.25 g (263 mmol; 1.05 eq) of cyanamide was placed is isopropanol (800 ml per tool of ethyl trifluoroacetoacetate; EtTFAA) at 50° C. and HCl gas (18.3 g; 500 mmol; 2.0 eq) was passed through the mixture for one hour. When the introduction of HCl had ended, the mixture was stirred for 2 hours at 70° C. It was then allowed to cool to room temperature and 3/4 of the solvent was evaporated off on a rotary evaporator. 80 ml of water (320 ml per mol of ethyl trifluoroacetoacetate) was added at room temperature to the O-isopropylisourea hydrochloride formed. Aqueous NaOH solution (78.87 g; 1.09 eq; 14 percent according to titration) was then added over 5 minutes at room temperature until the pH had shifted from 0.5 to 11.5, and stirring was continued for 15 minutes. The temperature was kept at ≤30° C. during the addition of the NaOH. Ethyl trifluoroacetoacetate (46.5 g; 500 mmol; 1.0 eq) was then added dropwise to this solution at room temperature. The temperature rose to 30° C. during this process and two phases formed. This mixture was refluxed for 2 hours. The organic solvents were then distilled off until the top temperature reached ca. 96° C. Stirring was continued for 2 hours at 85° to 90° C. The light yellow emulsion was allowed to cool to room temperature, the pH of 7.3 was adjusted to 5.0 with a small amount of 2 N aqueous HCl solution and the granular solid was filtered off after 20 minutes at room temperature. The moist solid obtained after filtration was taken up again with distilled water (~1 g moist product/ml water) and refluxed for 1 hour. After cooling to room temperature, filtration and drying, a light yellowish solid of relatively high content was obtained: the total yield was 67.8 percent (content: 98.0 percent according to HPLC). The solid was washed with a small amount of cold water and then dried overnight in a vacuum drying cabinet at 40° C. 41.3 g of a yellowish solid was obtained as the product, corresponding to a yield of 69.8 percent (content: 94.5 percent according to HPLC).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05717096 |
|---|
| Quelldatensatz | uspto-grants-1998_02 |
|---|
| ORD ID | ord-6a46d02dcd04422691238f61fd7e1c2f |
|---|
| Quellennotiz | uspto-grants-1998_02 |
|---|