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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453322Generated: October 29, 2026

Potassium Iodide → 1-[5-Chloro-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/453322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
Reactantethyl 1-[(5-chloro-2-hydroxyphenyl)methyl]-5-methyl-1H-pyrazole-3-carboxylateHCID 57875648—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-[5-Chloro-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazole-3-carboxylic acid ethyl esterHCID 8666728371%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 1-(5-Chloro-2-hydroxy-benzyl)-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester 2 (0.6 g, 2.0 mmol) in DMF (5 mL) were added potassium carbonate (0.84 g, 6.1 mmol), potassium iodide (0.34 g, 2.0 mmol) and 4-chlorobenzylbromide (0.38 g, 2.2 mmol). The resulting mixture was heated at 100° C. overnight. The mixture was poured into water (20 mL) and extracted with Et2O (3×15 mL). The organic layers were combined, washed with brine (30 mL), dried (Na2SO4) and the volatiles were removed in vacuo to give 0.56 g (71%) of 1-(2-Benzyloxy-5-chloro-benzyl)-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester 3 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492424B2
Source datasetuspto-grants-2013_07
ORD IDord-e850a4f913fd4d029228d14700a4bf10
Source noteuspto-grants-2013_07