HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 178463783, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aniline, N-(2-bromoethyl)-N-ethyl- | HCID 13228 | — |
| Reactant | Sodium Nitrate | HCID 24268 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Aminoimidazole hemisulfate | HCID 2734684 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178463783 | HCID 178463783 | 37.3% |
Reaction Steps
1.32 g 2-amino-1H-imidazol-hemisulfate is diazotized in a mixture containing 2 ml hydrochloric acid, 2 ml acetic acid, 12 ml water and 0.7 g sodium nitrate at 5° C. Azo coupling is performed by adding 2.3 g N-(2-bromoethyl)-N-ethylaniline to the above diazonium solution. After stirring for 2 hours at room temperature the mixture is poured on 50 ml saturated sodium bicarbonate. The resulted precipitate is filtered off, washed with water, and dried in vacuum at 40° C. After chromatography on silicagel with ethylacetate, 0.6 g N-(2-bromoethyl)-N-ethyl-4-[(E)-1H-imidazol-2-yldiazenyl]aniline is obtained as a brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07513916B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-41dcae07babd44b5b3ae8eef0537df68 |
| Source note | uspto-grants-2009_04 |