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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433588Generated: October 25, 2026

(3,4-Dichlorophenyl)hydrazine → 1-(3,4-dichloro-phenyl)-3-methyl-1H-pyrazole

https://huagongshe.com/reaction/433588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3,4-Dichlorophenyl)hydrazineHCID 83161—
Reactant4,4-Dimethoxy-2-butanoneHCID 228548—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-(3,4-dichlorophenyl)-5-methyl-1H-PyrazoleHCID 2344495029%
Product1-(3,4-dichloro-phenyl)-3-methyl-1H-pyrazoleHCID 2344503766%

Reaction Steps

A solution of of 3,4-dichlorophenylhydrazine (4.27 g, 20.0 mmol) in EtOH (50 ml) and H2O (50 ml) was treated with 3-oxobutyraldehyde dimethyl acetal (2.64 g, 20.0 mmol) and refluxed for 1 h. The alcohol was removed in vacuo and the aqueous residue was extracted with AcOEt (2×150 ml). The organic phase was dried (Na2SO4), filtered and evaporated. The remaining oil was chromatographed [silica, elution with gradient hexane to 10% (hexane/AcOEt=1:1)] to obtain 3.01 g (66%) of 1-(3,4-dichloro-phenyl)-3-methyl-1H-pyrazole [Mp. 57-58° C. (AcOEt/hexane), MS: m/e=226 (M+)] as off-white crystals and 1.32 g (29%) of 1-(3,4-dichloro-phenyl)-5-methyl-1H-pyrazole [Mp. 46-47° C. (hexane), MS: m/e=226 (M+)] as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667335B2
Source datasetuspto-grants-2003_12
ORD IDord-968d9223ab1b443e84dcf253fd57814f
Source noteuspto-grants-2003_12