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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511837Generated: November 1, 2026

Hydrochloric Acid → 1-methyl-6-(trifluoromethyl)-1H-indazole-3-carboxylic acid

https://huagongshe.com/reaction/511837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 1-methyl-6-(trifluoromethyl)-1H-indazole-3-carboxylateHCID 67291403—
SolventTetrahydrofuranHCID 8028—
Product1-methyl-6-(trifluoromethyl)-1H-indazole-3-carboxylic acidHCID 67289844—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a tetrahydrofuran (2 mL) of methyl 1-methyl-6-(trifluoromethyl)-1H-indazole-3-carboxylate (50 mg, 0.19 mmol) was added 2N sodium hydroxide (0.2 ml, 4.0 mmol) at room temperature. The mixture was refluxed at 90° C. with stirring for 3 hours. After being cooled to room temperature, 2N hydrochloric acid was added to the mixture until pH became 4.0. The organic layer was extracted with ethyl acetate, washed with brine, and dried over magnesium sulfate. After the filtration to separate solvent and magnesium sulfate, the solvent was removed under reduced pressure to give 47 mg (quantitative yield) of the title as a white solid that was used in the next step without further purification;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09101616B2
Source datasetuspto-grants-2015_08
ORD IDord-6579fd8e7f644ad7aa00b6a1c1a42870
Source noteuspto-grants-2015_08