HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetamidine → Ethyl 2,4-bis(trifluoromethyl)pyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetamidine | HCID 2776882 | — |
| Reactant | Ethyl 2-(ethoxymethylene)-4,4,4-trifluoro-3-oxobutanoate | HCID 4685753 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2,4-bis(trifluoromethyl)pyrimidine-5-carboxylate | HCID 10493558 | 39% |
Reaction Steps
A solution of ethyl ethoxymethylene-4,4,4-trifluoroacetoacetate (15 g, 62.5 mmol) and trifluoroacetamidine (12.6 g, 112.5 mmol) in EtOH (50 mL) was heated at reflux for 24 h under N2. The reaction mixture was cooled and concentrated. Chromatography (SiO2, 20% EtOAc/hexane) afforded ethyl-2,4-bis (trifluoromethyl)pyrimidine-5-carboxylate as an oil (7.0 g, 39%), 1HNMR (CDCl3) δ 9.37 (s, 1H), 3.70 (q, 2H), 1.27 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811428 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-4baead46329c48d7a417b6270e76d3e4 |
| Source note | uspto-grants-1998_09 |