HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Hydroxy-3-(3-nitrobenzyl)-2,4-dioxoimidazolidine-1-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 7219893 | HCID 7219893 | — |
| Reactant | 3-(3-Nitrobenzyl)-4,5-dioxo-2-thioxoimidazolidine-1-acetic acid | HCID 10639626 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Hydroxy-3-(3-nitrobenzyl)-2,4-dioxoimidazolidine-1-acetic acid | HCID 10638590 | — |
Reaction Steps
The above-prepared dioxoimidazolidine-1-acetate product of paragraph (2) (15 g) was suspended in a mixed solvent of acetic acid and hydrochloric acid and the mixture was heated to reflux with stirring for two hours. Then the mixture was concentrated in vacuo, ether-chloroform was added thereto. The crystals were dislodged from the wall of the reaction flask with a spatula. The solid was washed with ether and recrystallized from a mixed solvent of ethanol and water to give 8.1 g of 5-hydroxy-3-(3-nitrobenzyl)-2,4-dioxoimidazolidine-1-acetic acid [Compound 15]. The melting point, MS, IR, NMR, and elementary analysis for the compound were:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05912261 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-e290105a68214f799ce679b4b7df143e |
| Source note | uspto-grants-1999_06 |