HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzaldehyde → 2-[(E)-2-(4-Nitrophenyl)ethenyl]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Methylpyridine | HCID 7975 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Product | 2-[(E)-2-(4-Nitrophenyl)ethenyl]pyridine | HCID 5376482 | — |
Reaction Steps
A solution of 46.5 g (0.5 mole) of 2-methylpyridine and 75.5 g (0.5 mole) of 4-nitrobenzaldehyde in about 100 g of acetic anhydride (about 1 mole) is refluxed for 6 hours, after which it is carefully poured onto ice water. The stirred mixture is neutralized with saturated, aqueous sodium bicarbonate solution. The precipitate is filtered off under suction, washed with water and recrystallized from ethanol to give 66 g (63% of theory) of reddish brown crystals of melting point 136°-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04897425 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-82de892bb1634cf598b353607d58ea6b |
| Source note | uspto-grants-1990_01 |