HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256358Generated: October 29, 2026
Ethanol → Ethyl 2,2-dimethyl-5-oxo-1-imidazolidineacetate
https://huagongshe.com/reaction/256358
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium 2,2-dimethyl-5-oxo-1-imidazolidineacetate | HCID 23686064 | — |
| Product | Ethyl 2,2-dimethyl-5-oxo-1-imidazolidineacetate | HCID 53986652 | — |
Reaction Steps
(1) To an ice-cold solution of thionyl chloride (5 ml) in dry ethanol (50 ml) a solution of sodium 2,2-dimethyl-5-oxo-1-imidazolidineacetate (4 g) in dry ethanol (50 ml) was added dropwise. The mixture was stirred at 0° C. for 1 hour, then at room temperature overnight. After evaporation under reduced pressure, the residue was taken up with a saturated solution of sodium hydrogen carbonate and extracted with 3×100 ml of dichloromethane. The organic layer was dried and evaporated, to yield ethyl 2,2-dimethyl-5-oxo-1-imidazolidineacetate (2.57 g) as a colorless oil (Rf. 0.49, methanol/acetone 1:1; silica gel plates). Oxalate salt m.p. 109°-113° C. (ethanol/diethyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04703054 |
|---|
| Source dataset | uspto-grants-1987_10 |
|---|
| ORD ID | ord-84e623737adb4623a366e29015fa09fa |
|---|
| Source note | uspto-grants-1987_10 |
|---|