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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781873Generated: October 31, 2026

Hydrazine hydrate (1:1) → HCID 178526459, compound

https://huagongshe.com/reaction/1781873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantEthyl(3,4-dihydroxy-5-nitrobenzoyl)acetateHCID 21459116—
SolventEthanolHCID 702—
ProductHCID 178526459HCID 178526459—

Reaction Steps

2.0 g of ethyl (3,4-dihydroxy-5-nitrobenzoyl)acetate are suspended in 50 ml of ethanol. After treatment with 0.4 g of hydrazine hydrate the mixture is held at the reflux temperature for 16 hours. After distillation of the solvent, the residue is held at the boiling temperature for 5 minutes with 50 ml of ethyl acetate. The separated precipitate is filtered under suction and the filtrate is concentrated to 10 ml. The crystals, which separate in the cold, are filtered under suction. There is obtained 5-(5-hydroxypyrazol-3-yl)-3-nitropyrocatechol in form of orange crystals of m.p. 228° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633371
Source datasetuspto-grants-1997_05
ORD IDord-6445255240324e9d8447953c0b0e269b
Source noteuspto-grants-1997_05