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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073238Generated: October 26, 2026

Hydrazine hydrate (1:1) → 4-Benzoyl-2-nitrophenylhydrazine

https://huagongshe.com/reaction/2073238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-Chloro-3-nitrobenzophenoneHCID 41743—
SolventEthanolHCID 702—
Product4-Benzoyl-2-nitrophenylhydrazineHCID 1985812875%

Reaction Steps

20 ml of hydrazine hydrate were added to the suspension of 52.33 g of 4-chloro-3-nitrobenzophenone in 200 ml of abs. ethanol under stirring. The reaction mixture was stirred at room temperature for 75 minutes, then slowly heated to the boiling point. After completion of the violent reaction, the mixture was refluxed for an additional 1 hour. After cooling down, the crystals were filtered by suction, thoroughly washed with water and dried at 80° C. Thus, 38.62 g (75%) of 4-benzoyl-2-nitrophenylhydrazine were obtained as orange-red crystals, m.p.: 163°-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04916149
Source datasetuspto-grants-1990_04
ORD IDord-61633c24326744f5aeb3a541f73adf4b
Source noteuspto-grants-1990_04