HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 178437682, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 178437684 | HCID 178437684 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178437682 | HCID 178437682 | — |
Reaction Steps
864 mg (2 mmol) of 1-(benzylideneamino)-3-(p-chlorophenacyl)-2-ethylimidazolium bromide are subjected to a steam distillation in 5 ml of water and 2 ml of 48 percent hydrobromic acid until benzaldehyde no longer evolves. The solution is concentrated and te precipitated product is filtered off. There is obtained 1-amino-3-(p-chlorophenacyl)-2-ethylimidazolium bromide of melting point 209°-210°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831151 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-aab31ccb41c84970b568a94ff09dc9d9 |
| Source note | uspto-grants-1989_05 |