HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Aminohydantoin → alpha-[[[(2,4-Dioxo-1-imidazolidinyl)amino]carbonyl]amino]benzeneacetic acid, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Aminohydantoin | HCID 72823 | — |
| Reactant | alpha-Isocyanatobenzeneacetic acid, ethyl ester | HCID 56982438 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | alpha-[[[(2,4-Dioxo-1-imidazolidinyl)amino]carbonyl]amino]benzeneacetic acid, ethyl ester | HCID 86734963 | — |
Reaction Steps
1.15 g. (0.01 mol.) of 1-amino-2,4-dioxoimidazolidine are dissolved in 50 ml. of dioxane while heating. The solution is permitted to cool to room temperature while stirring, wherein a portion of the 1-amino-2,4-dioxoimidazolidine crystallizes out. 2.05 g. (0.01 mol.) of α-isocyanatobenzeneacetic acid, ethyl ester are added and the reation mixture is stirred overnight at room temperature. On the next day the mixture is concentrated and the residue is triturated with ether. 3.0 g. of α-[[[(2,4-dioxo-1-imidazolidinyl)amino]-carbonyl] amino]benzeneacetic acid, ethyl ester are obtained, m.p. 148°-151°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04038271 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-5135711ffbba467f97cb00c6db5a74f4 |
| Source note | uspto-grants-1977_07 |