HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 54158128, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 86743482 | HCID 86743482 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54158128 | HCID 54158128 | — |
Reaction Steps
37.6 g of 6-nitro-2-styrylquinoline-6-nitroquinaldine, 21.2 g of benzaldehyde and 20.4 g of acetic anhydride were mixed and heated for 5 hours under reflux. After the reaction mixture was allowed to cool, 100 ml of ethyl acetate were added thereto and the deposited crystals were filtered. 41.6 g (75% of the theoretical yield) of the 6-nitro-2-styrylquinoline crystals were produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04877723 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-f30b612719434375b0cbf57e4200ce4e |
| Source note | uspto-grants-1989_10 |