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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172697Generated: October 25, 2026

Water → HCID 59556309, compound

https://huagongshe.com/reaction/1172697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,4,5-TrifluorobenzonitrileHCID 593813—
Reactant1-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propan-1-olHCID 23549129—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59556309HCID 5955630995.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 900 mg of 1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propan-1-ol in 2 mL of tetrahydrofuran at 5° C. was slowly added 3.3 mL of a molar solution of potassium tert-butoxide in tert-butanol. After stirring at 5° C. for 30 minutes, the resulting solution was slowly added to a solution of 469 mg of 2,4,5-trifluoro-benzonitrile in 2 mL of tetrahydrofuran at −60° C. The resulting mixture was stirred for 1 h at −60° C. then stirred overnight allowing the temperature to warm up to room temperature. It was then poured into water and extracted with dichloromethane. The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel (gradient from heptane 100 to heptane 80/ethyl acetate 20) to give 1.25 g of 2,5-difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834030B2
Source datasetuspto-grants-2010_11
ORD IDord-640d9a37120e4412a9ff258c71214264
Source noteuspto-grants-2010_11