HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-[1-(4-Nitrophenyl)ethylidene]malononitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | p-Nitroacetophenone | HCID 7487 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[1-(4-Nitrophenyl)ethylidene]malononitrile | HCID 11042086 | 48.7% |
Reaction Steps
A mixture of 1-(4-nitrophenyl)ethanone (15 g, 90.8 mmol), malononitrile (6 g, 90.8 mmol), ammonium acetate (7 g, 90.8 mmol) and acetic acid (10 mL) in benzene (200 mL) was stirred at reflux overnight in a flask equipped with a Dean-Stark trap. The reaction mixture was cooled to room temperature, poured into water, and extracted three times with ethyl acetate. The combined organic extracts were washed with water and brine, dried (MgSO4), filtered, and concentrated. The residue was purified by silica gel chromatography eluting with 25% ethyl acetate/hexanes to provide 9.42 g of the desired product. Rf=0.33 (25% ethyl acetate/hexanes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560552B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-bd1a019f50e3463480e2a636828d3f82 |
| Source note | uspto-grants-2009_07 |