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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491850Generated: October 29, 2026

Bromine → 3-(4-Bromo-pyrazol-1-yl)-4-methyl-benzoic acid ethyl ester

https://huagongshe.com/reaction/491850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant4-Methyl-3-pyrazol-1-yl-benzoic acid ethyl esterHCID 58861336—
SolventChloroformHCID 6212—
Product3-(4-Bromo-pyrazol-1-yl)-4-methyl-benzoic acid ethyl esterHCID 58861442102.6%

Reaction Steps

A solution of 3-hydrazino-4-methyl benzoic acid (1.0 g, 4.93 mmol), malonaldehyde(bismethylacetate) (0.82 mL, 4.93 mmol), and concentrated HCl (1 mL) in EtOH (20 mL) was heated to reflux for 4 h. After cooling to room temperature, the reaction was poured into ice water, neutralized with 2N NaOH, and extracted with CH2Cl2 (3×). The organic layers were dried over Na2SO4, filtered and concentrated to afford 4-methyl-3-pyrazol-1-yl-benzoic acid ethyl ester (536 mg, 47%) as a yellow oil. A solution of the pyrazole (536 mg, 2.33 mmol) and bromine (0.167 mL, 3.26 mmol) in CHCl3 (15 mL) was refluxed for 4.5 h then cooled to room temperature. The solvent was evaporated to an orange oil. Purification using chromatography on silica gel (1:1 EtOAc/hexanes) yielded 3-(4-bromo-pyrazol-1-yl)-4-methyl-benzoic acid ethyl ester (0.739 g, 99%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531560B2
Source datasetuspto-grants-2009_05
ORD IDord-4b7d59e09c434d6bbef4f7c458658181
Source noteuspto-grants-2009_05