HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(3,5-Dibromophenyl)-1-phenyl-1h-benzo[d]imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-Phenyl-o-phenylenediamine | HCID 68297 | — |
| Reactant | 3,5-Dibromobenzaldehyde | HCID 622077 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(3,5-Dibromophenyl)-1-phenyl-1h-benzo[d]imidazole | HCID 59439661 | — |
Reaction Steps
20 g (75.8 mmol) of 3,5-dibromobenzaldehyde and 16.8 g (90.9 mmol) of N-phenyl-o-phenylenediamine were dissolved in 150 mL of acetic acid. The solution was agitated at room temperature for 30 minutes. Next, 37 g (83.4 mmol) of lead(IV) acetate was added thereto. The resulting product was agitated at 50° C. for 1 hour. Then, water was poured into the obtained reactant. The resulting product was treated with ethyl acetate to perform extraction and the solvent was removed under a reduced pressure. The extract was separated through a column and dried, obtaining 9.5 g (Y=29%) of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772632B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-33fbacba96104733ae9428a27f656587 |
| Source note | uspto-grants-2014_07 |