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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867567Generated: November 1, 2026

Hydrazine hydrate (1:1) → HCID 135519368, compound

https://huagongshe.com/reaction/1867567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 11416722HCID 11416722—
CatalystSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
ProductHCID 135519368HCID 135519368—

Reaction Conditions

Temperature70 °C

Reaction Steps

6-Chloro-7-hydroxy-3-(4methoxy-phenyl)-4-oxo-4H-chromene-2-carboxylic acid (1 eq) was taken up in ethanol and hydrazine hydrate (3 eq) was added. To aid dissolution a few drops of NaHCO3 (aq) was added, and then all was heated at 70° C. under nitrogen for 2 hours. The solution was cooled to room temperature and concentrated in vacuo to a brown oil. This was partitioned between 1MHCl(aq) and diethyl ether. The organic phases were combined, washed with 1MHCl(aq), dried over MgSO4, filtered and concentrated in vacuo to give 5-(5-chloro-2,4dihydroxy-phenyl)-4-(4-methoxy-phenyl)-2H-pyrazole-3-carboxylic acid as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632855B2
Source datasetuspto-grants-2009_12
ORD IDord-e28302da3592433696f6ec7d8b64caf9
Source noteuspto-grants-2009_12