Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257410Generated: November 1, 2026

Hydrochloric Acid → 5-(trifluoromethyl)-1-({4-[3-(trifluoromethyl)phenyl]-1,3-thiazol-2-yl}methyl)-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1257410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactantethyl 5-(trifluoromethyl)-1-({4-[3-(trifluoromethyl)phenyl]-1,3-thiazol-2-yl}methyl)-1H-pyrazole-4-carboxylateHCID 86650597—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-(trifluoromethyl)-1-({4-[3-(trifluoromethyl)phenyl]-1,3-thiazol-2-yl}methyl)-1H-pyrazole-4-carboxylic acidHCID 8665059898.5%

Reaction Steps

A mixture of the compound (0.13 g) obtained in Example 103d, 4N sodium hydroxide (1 mL), ethanol (2 mL) and tetrahydrofuran (0.5 mL) was stirred at room temperature for 20 hr. The reaction mixture was adjusted to pH 5 with 1N hydrochloric acid, and ethyl acetate and water were added. The ethyl acetate layer was separated, dried over sodium sulfate, and concentrated under reduced pressure to give the title compound (0.12 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461348B2
Source datasetuspto-grants-2013_06
ORD IDord-ab95609c0d4a4112886b0f29930c2cf8
Source noteuspto-grants-2013_06