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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767882Generated: October 25, 2026

[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-acetic acid → 2-[4-Methyl-2-[4-(trifluoromethyl)phenyl]-5-thiazolyl]ethanol

https://huagongshe.com/reaction/1767882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-acetic acidHCID 17972178—
SolventTetrahydrofuranHCID 8028—
Product2-[4-Methyl-2-[4-(trifluoromethyl)phenyl]-5-thiazolyl]ethanolHCID 22647583100%

Reaction Steps

A solution of [4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-acetic acid (6.01 g, 20 mmol) in tetrahydrofuran (180 ml) was treated at 0° C. with a 1 M solution of BH3*THF in tetrahydrofuran (49.8 ml, 49.8 mmol). The cooling bath was removed and the reaction mixture stirred at ambient temperature for 16 h. Careful quenching with MeOH and ice water, twofold extraction with AcOEt, washing with ice water/brine 1/1, drying over magnesium sulfate, and evaporation of the solvent left a crude product which was refluxed for 30 min in MeOH to liberate quantitatively the free alcohol. The solvent was evaporated in vacuo and the residue was purified by column chromatography (silica gel, dichloromethane/MeOH) to yield 5.68 g (20 mmol, 99%) of the title compound as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235572B2
Source datasetuspto-grants-2007_06
ORD IDord-b67eaf779c8842e9b4efb23589e28b78
Source noteuspto-grants-2007_06