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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733121Generated: October 30, 2026

3-Bromophenylhydrazine hydrochloride → Ethyl 1-(3-bromophenyl)-5-methyl-1h-pyrazole-3-carboxylate

https://huagongshe.com/reaction/733121

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromophenylhydrazine hydrochlorideHCID 33757—
ReactantEthyl 2,4-dioxovalerateHCID 69208—
SolventAcetic AcidHCID 176—
ProductEthyl 1-(3-bromophenyl)-5-methyl-1h-pyrazole-3-carboxylateHCID 1854927785%

Reaction Steps

A solution of 3-bromophenylhydrazine hydrochloride (2 g, 8.9 mmol) and ethyl-2,4-dioxovalerate (1.69 g, 10.7 mmol) in acetic acid (44 ml) was refluxed for 16 hours. The reaction was cooled to room temperature and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The organic layer was washed with water, saturated bicarbonate and brine, and then dried over sodium sulfate, filtered and concentrated in vacuo. The crude product, thus obtained, was purified by silica-gel column chromatography (4.8:0.2 hexanes/ethyl acetate) to give the product (2.34 g, 84%) as a syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589116B2
Source datasetuspto-grants-2009_09
ORD IDord-4bd1734b898549f9ae0564afeda9c50e
Source noteuspto-grants-2009_09