HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1,4-Bis(2-carbethoxy-2-cyano-1-methylethenyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | 1,4-Diacetylbenzene | HCID 13888 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,4-Bis(2-carbethoxy-2-cyano-1-methylethenyl)benzene | HCID 3393270 | — |
Reaction Steps
A mixture of p-diacetylbenzene (20.25 g, 0.125 mole), ethyl cyanoacetate (28.3 g, 0.25 mole), ammonium acetate (3.85 g) and acetic acid (10 g) was combined in a 500 ml glass round-bottom flask with toluene (150 ml) and refluxed for 12 hours. A Dean-Stark trap was employed to trap water formed during the reaction. Refluxing was discontinued and the solvent evaporated. The residue containing crude product was distilled under reduced pressure. One fraction, boiling point range 177° C.-195° C. (0.6 mm) amounting to 20.6 g was identified as predominately the 1:1 condensation product. A second fraction, boiling point ~200° C. yielded 18.2 g of 1,4-bis(2-carbethoxy-2-cyano-1-methylethenyl)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04263209 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-d764701e8bc64cfb8a45efabc7211bdc |
| Source note | uspto-grants-1981_04 |