HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-(4-Chlorophenyl)-4-oxocyclohexanecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Carbomethoxy-4-(p-chlorophenyl)-4-cyanocyclohexanone | HCID 12230234 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Chlorophenyl)-4-oxocyclohexanecarbonitrile | HCID 12230238 | 82% |
Reaction Steps
A mixture of 29.8 g. (0.102 mole) of methyl 5-cyano-5-(4-chlorophenyl)-2-oxocyclohexanecarboxylate (prepared in Example 7) in 660 ml. of acetic acid and 330 ml. of 10% sulfuric acid is stirred mechanically on a steam bath for about 24 hours. The mixture is then allowed to cool and diluted with water. This mixture is extracted thoroughly with benzene. The organic layer is washed successively with water, sodium bicarbonate solution and brine and evaporated to dryness. The solid residue is recrystallized from ether to give 19.49 g. (82% yield) of 4-cyano-4-(4-chlorophenyl)cyclohexanone, having a melting point of 94.5° to 97°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03979444 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-0f1876c50e4744a7893575c4349be497 |
| Source note | uspto-grants-1976_09 |