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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-methoxy-1-methyl-5-trifluoromethyl-1H-pyrazole | HCID 17862856 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-chloromethyl-3-methoxy-1-methyl-5-trifluoromethyl-1H-pyrazole | HCID 17862881 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833939B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-b511b0ec2d1a48a0a3e96c4b48d7ed1b |
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| Source note | uspto-grants-2010_11 |
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