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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172107Generated: October 26, 2026

Hydrochloric Acid → 4-chloromethyl-3-methoxy-1-methyl-5-trifluoromethyl-1H-pyrazole

https://huagongshe.com/reaction/1172107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantPotassium CarbonateHCID 11430—
Reactant3-methoxy-1-methyl-5-trifluoromethyl-1H-pyrazoleHCID 17862856—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product4-chloromethyl-3-methoxy-1-methyl-5-trifluoromethyl-1H-pyrazoleHCID 1786288165%

Reaction Conditions

Temperature80 °C

Reaction Steps

0.45 g of paraformaldehyde (15.0 mmoles in terms of formaldehyde) and 5 ml of concentrated hydrochloric acid were added to a solution of 1.00 g (5.6 mmoles) of 3-methoxy-1-methyl-5-trifluoromethyl-1H-pyrazole dissolved in 25 ml of acetic acid. The mixture was stirred at 80° C. for 2 hours to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water and neutralized with potassium carbonate, followed by extraction with ethyl acetate. The resulting organic layer was washed with water and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein. The residue was purified by silica gel column chromatography (developing solvent: hexane-ethyl acetate mixed solvent) to obtain 0.83 g (yield: 65.0%) of 4-chloromethyl-3-methoxy-1-methyl-5-trifluoromethyl-1H-pyrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-b511b0ec2d1a48a0a3e96c4b48d7ed1b
Source noteuspto-grants-2010_11