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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086747Generated: November 1, 2026

Pyrazole → methyl 2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoate

https://huagongshe.com/reaction/1086747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactant2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoic acidHCID 15671959—
SolventAcetoneHCID 180—
Productmethyl 2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoateHCID 1567196048%

Reaction Steps

A KOH powder (0.1 g, 1.8 mmoles) and methyl iodide (0.26 g, 1.8 mmols) were added to a solution of 2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoic acid (0.30 g, 0.8 moles) in 20 ml acetone and reacted with this pyrazole derivative under reflux 3 hours. Then the extraction with ethylacetate, washing with water, dehydration, and concentration of the extract solution, and purification of the residue by column chromatography gave the title compound (0.15 g), yield 48%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05032165
Source datasetuspto-grants-1991_07
ORD IDord-b96d1263fd3f420ab8aa073eec8e0ecb
Source noteuspto-grants-1991_07