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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1172697Erstellt: 26. Oktober 2026

Water → HCID 59556309, Verbindung

https://huagongshe.com/reaction/1172697

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2,4,5-TrifluorobenzonitrileHCID 593813—
Edukt1-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propan-1-olHCID 23549129—
EduktPotassium tert-butoxideHCID 23665647—
Lösungsmitteltert-ButanolHCID 6386—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 59556309HCID 5955630995,5%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07834030B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-640d9a37120e4412a9ff258c71214264
Quellennotizuspto-grants-2010_11