HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-(2-Aminoacetyl)-2,2-dimethyl-5-oxo-1-imidazolidine acetamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3-(2-Chloroacetyl)-2,2-dimethyl-5-oxo-1-imidazolidineacetamide | HCID 20163752 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(2-Aminoacetyl)-2,2-dimethyl-5-oxo-1-imidazolidine acetamide hydrochloride | HCID 20163705 | — |
Reaction Steps
A suspension of 3-(2-chloroacetyl)-2,2-dimethyl-5-oxo-1-imidazolidineacetamide (0.48 g) in 33% ammonia solution (6 ml) was stirred at room temperature for 90 minutes. The clear solution obtained was diluted with dry ethanol (80 ml) and evaporated under reduced pressure. The residue was crystallized from water/acetone to afford 3-(2-aminoacetyl)-2,2-dimethyl-5-oxo-1-imidazolidine acetamide hydrochloride as a white powder, m.p. 292° C. decomp.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04703054 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-0eab3dbadc7548d7ba5172fcd67d59c9 |
| Source note | uspto-grants-1987_10 |