HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamidine acetate → HCID 19735286, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Diethyl [o-(trifluoromethyl)benzyl]malonate | HCID 53709043 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19735286 | HCID 19735286 | — |
Reaction Steps
0.63 g of formamidine acetate in 40 ml of absolute ethyl alcohol was treated with 1.2 g of sodium ethylate at room temperature, stirred at room temperature for 30 minutes and then treated dropwise at room temperature with a solution of 1.6 g of diethyl [o-(trifluoromethyl)benzyl]malonate in 8 ml of absolute ethyl alcohol. After stirring at 50° C. for 4 hours, the reaction mixture was worked-up and yielded 5-[o-(trifluoro-methyl)benzyl]-4,6(1H,5H)pyrimidinedione, melting point >290° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05270313 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-447e051c1f574ccc9b08459938f456dc |
| Source note | uspto-grants-1993_12 |