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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867382Generated: October 31, 2026

Hydroxide → HCID 13882133, compound

https://huagongshe.com/reaction/867382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxideHCID 961—
ReactantEthyl 1-(3-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylateHCID 13772950—
SolventEthanolHCID 702—
ProductHCID 13882133HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775409
Source datasetuspto-grants-1988_10
ORD IDord-2e1224490ec44c9194dbd7858ff306ac
Source noteuspto-grants-1988_10