HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamidine monohydrochloride → Ethyl (2-Methyl-6-trifluoromethyl-3H-pyrimidin-4-on-5-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Butanedioic acid, (trifluoroacetyl)-, diethyl ester | HCID 11346247 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl (2-Methyl-6-trifluoromethyl-3H-pyrimidin-4-on-5-yl)acetate | HCID 136102355 | 27% |
Reaction Steps
A mixture of NaOEt (0.074 mol) in EtOH (prepared from 1.7 g of Na and 75 mL of EtOH), acetamidine hydrochloride (3.5 g, 0.037 mol), and diethyl 2-trifluoroacetylsuccinate (10.0 g, 0.037 mol) was heated under reflux for 20 h. The mixture was concentrated, taken up in water, acidified to pH 4 with conc. HCl, and extracted with EtOAc. The extracts were washed with brine, dried (MgSO4), and concentrated to give an oily solid. Trituration with ether/hexane gave 2.63 g (27%) of product as a white solid. An analytical sample was recrystallized from ether/hexane, mp 108°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05149699 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-dc542d7b62c8437ba9bf73d27bf9a6cb |
| Source note | uspto-grants-1992_09 |