HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxide → HCID 13882133, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxide | HCID 961 | — |
| Reactant | Ethyl 1-(3-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylate | HCID 13772950 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13882133 | HCID 13882133 | — |
Reaction Steps
A 14 g. portion of ethyl 1-(3-bromophenyl)-5-cyano-4-pyrazolecarboxylate was hydrolyzed by stirring under reflux in 200 ml. of ethanol with 6 g. ofpotassium hydroxide for 2 hours. The mixture was then poured over ice, acidified and filtered, and the solids were crystallized from ethanol/water and dried at 168° to obtain 10 g. of the desired product, m.p. 215°-217° dec. The product was identified by NMR analysis in CDCl3 /DMSOd6. δ7.06 (s, 1), carboxamide; 7.30-7.64 (m, 4), aromatic; 8.08 (s, 1), pyrazole; 9.10 (s, 1), carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04775409 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-2e1224490ec44c9194dbd7858ff306ac |
| Source note | uspto-grants-1988_10 |