HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-(4-Fluorobenzylidene)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzene | HCID 241 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4-Fluorobenzylidene)aniline | HCID 918392 | — |
Reaction Steps
To 4-fluorobenzaldehyde (24.8 g, 0.200 mol) and aniline (18.6 g, 0.200 mol) was added benzene (200 mL) and acetic acid (0.7 mL) and the mixture is heated under reflux until all the water (3.6 mL) was azeotropically removed. The solvent is evaporated and the residual oil upon cooling and stirring crystallized. The white mass was then recrystallized as needles (28 g, 70%): mp 39°-40° C. (PE) (lit.1 mp 40° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374701 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-fa25214b4cea40cab83e37faa36aecfd |
| Source note | uspto-grants-1994_12 |