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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49641Generated: October 25, 2026

Hydrochloric Acid → 1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/49641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
Reactant1H-Pyrazole-4-carboxylic acid, 1-methyl-3-(trifluoromethyl)-, ethyl esterHCID 2782970—
SolventWaterHCID 962—
Product1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acidHCID 277566598.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

50 g of ethyl 1-methyl-3-trifluoromethyl-4-pyrazolecarboxylate were initially charged with 177 g of toluene and 54 g of 25% sodium hydroxide solution and heated to reflux for 15 hours. The cloudy reaction mixture was cooled to 50° C. and admixed with 69 g of water. The aqueous phase was adjusted to pH 1-2 at 30° C. by adding 83 g of 15% hydrochloric acid, and the product precipitated out of solution. The suspension was stirred for a further 30 minutes at room temperature and for 30 minutes at 0° C., and the crude product was then isolated and washed 3 times with 60 g each time of cold (<10° C.) water. After drying at room temperature and under reduced pressure, 43 g of 1-methyl-3-trifluoromethyl-4-pyrazolecarboxylic acid were obtained. This corresponds to a yield of 98% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706911B1
Source datasetuspto-grants-2004_03
ORD IDord-768d08ef2f7f472a83947b43f7b993f8
Source noteuspto-grants-2004_03