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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758773Generated: November 2, 2026

Hydrazinecarboxaldehyde, 2-(4-nitrophenyl)- → Hydrazinecarboxaldehyde, 2-(4-aminophenyl)-

https://huagongshe.com/reaction/1758773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazinecarboxaldehyde, 2-(4-nitrophenyl)-HCID 5008489—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHydrazinecarboxaldehyde, 2-(4-aminophenyl)-HCID 11318981.9%

Reaction Steps

In 1,600 ml of ethanol, 30 g of 2-(4-nitrophenyl)-1-formylhydrazine was catalytically reduced at room temperature, using palladium-carbon as a catalyst. The reaction mixture was filtered and the filtrate was evaporated to dryness, whereby 20.5 g of white solid 2-(4-aminophenyl)-1-formylhydrazine was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374923
Source datasetuspto-grants-1983_02
ORD IDord-e3c53cff41644ef2a1423e9b3b249b38
Source noteuspto-grants-1983_02