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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244622Generated: October 30, 2026

Hydrochloric Acid → 1-methyl-4-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid

https://huagongshe.com/reaction/244622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiazomethaneHCID 9550—
Reactant1,4-DioxaneHCID 31275—
ReactantEthyl 4,4,4-trifluoro-2-butynoateHCID 3597254—
CatalystHydrochloric AcidHCID 313—
Product1-methyl-4-(trifluoromethyl)-1H-pyrazole-5-carboxylic acidHCID 58356379—

Reaction Steps

To a solution of diazomethane (0.781 g—generated from DIAZALD® (3.99 g) in diethyl ether (63 ml)), cooled by an ice/water bath, was added ethyl 4,4,4-trifluoro-2-butynoate (3.09 g) dropwise over 1 min. The cooling bath was removed and the mixture was stirred for 30 min when the solvent was removed under reduced pressure. The crude product was combined with the crude product from a similar experiment that was performed with 1,4 dioxane (5 ml) and n-pentane (15 ml) as the solvent and purified by column chromatography on silica gel to give a white solid. To a solution of a portion of this solid (100 mg) in 1,4-dioxane (2 ml) was added 2M hydrochloric acid (3 ml) and the mixture heated at reflux for 18 h, then concentrated hydrochloric acid (2 drops) was added and the mixture heated at reflux for a further 48 h. The mixture was concentrated in vacuo and the residue purified by mass directed preparative HPLC (Method A), to give the title compound, as a white solid (19 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658635B2
Source datasetuspto-grants-2014_02
ORD IDord-ae028aed0dd04777984e1d91f8dabe8f
Source noteuspto-grants-2014_02