HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(4-Chlorophenyl)-5-cyano-1H-pyrazole-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 1-(4-chlorophenyl)-5-cyano-1H-pyrazole-4-carboxylate | HCID 13772949 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Chlorophenyl)-5-cyano-1H-pyrazole-4-carboxylic acid | HCID 13654127 | 83.4% |
Reaction Steps
A hot solution of 5.61 g of potassium hydroxide dissolved in 110 ml of 3A ethanol was added to a hot solution of 11.3 g of 5-cyano-1-(4-chlorophenyl)-1H-pyrazole-4-carboxylic acid, ethyl ester dissolved in 225 ml of 3A ethanol. The precipitated salt that was formed was dissolved into 1 liter of water and the solution was acidified with concentrated hydrochloric acid. The precipitated solid was collected by filtraton and recrystallized from toluene to provide 8.47 g of 5-cyano-1-(4-chlorophenyl)-1H-pyrazole-4-carboxylic acid. MP=192°-195° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04589905 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-910ee7b93a1143f398614f811ad85168 |
| Source note | uspto-grants-1986_05 |