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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233551Generated: November 1, 2026

Water → 2-[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-ethanol

https://huagongshe.com/reaction/2233551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-acetic acidHCID 59296126—
SolventTetrahydrofuranHCID 8028—
Product2-[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-ethanolHCID 5929616999.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.15 g crude [4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-acetic acid were dissolved in 50 ml tetrahydrofuran and cooled in an ice bath to 0° C. At 0° C. 9.3 ml 1 M solution of borane tetrahydrofuran complex were added. The reaction mixture was warmed to 55° C. and stirred for one hour at this temperature. The reaction mixture was cooled in an ice bath and 50 ml water was added. The organic layer was added. The tetrahydrofuran was removed in vacuo and the residue extracted three times with portions of 80 ml ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and the solvent removed in vacuo to provide 1.1 g crude 2-[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-ethanol as brown oil. This material was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709509B2
Source datasetuspto-grants-2010_05
ORD IDord-5286291971bf4f279c1742890c3204cf
Source noteuspto-grants-2010_05