Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296956Generated: October 30, 2026

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

https://huagongshe.com/reaction/1296956

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-(4-methoxy-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 1M HCl (aq) and diethyl ether. The organic phases were combined, washed with 1M HCl (aq), dried over MgSO4, filtered and concentrated in vacuo to give 5-(5-chloro-2,4-dihydroxy-phenyl)-4-(4-methoxy-phenyl)-2H-pyrazole-3-carboxylic acid as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247734B2
Source datasetuspto-grants-2007_07
ORD IDord-98a05657a50a4ebb8193f511c258c0f6
Source noteuspto-grants-2007_07