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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172105Generated: November 3, 2026

Acetic Acid → 1-tert-butyl-4-chloromethyl-5-methoxy-3-trifluoromethyl-1H-pyrazole

https://huagongshe.com/reaction/1172105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
Reactant1-tert-butyl-5-methoxy-3-trifluoromethyl-1H-pyrazoleHCID 17862917—
Product1-tert-butyl-4-chloromethyl-5-methoxy-3-trifluoromethyl-1H-pyrazoleHCID 1786290989%

Reaction Conditions

Temperature60 °C

Reaction Steps

5.4 g of paraformaldehyde (180.2 mmoles in terms of formaldehyde) and 20 ml of concentrated hydrochloric acid were added to a solution of 20.0 g (90.1 mmoles) of 1-tert-butyl-5-methoxy-3-trifluoromethyl-1H-pyrazole dissolved in 90 ml of acetic acid. The mixture was stirred at 60° C. for 30 minutes to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water, followed by extraction with diisopropyl ether. 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, to obtain 21.7 g (yield: 89.0%) of 1-tert-butyl-4-chloromethyl-5-methoxy-3-trifluoromethyl-1H-pyrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-c120315f45f848da9cb9706716b3fbe3
Source noteuspto-grants-2010_11