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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2096833Erstellt: 25. Oktober 2026

(Trifluoromethyl)trimethylsilane → 6-[2-(4-Bromo-2-chloro-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-3-methyl-3H-benzooxazol-2-one

https://huagongshe.com/reaction/2096833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(Trifluoromethyl)trimethylsilaneHCID 552549—
EduktTetrabutylammonium Fluoride TrihydrateHCID 11726816—
Edukt6-[2-(4-Bromo-2-chloro-phenyl)-propionyl]-3-methyl-3H-benzooxazol-2-oneHCID 66697107—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-[2-(4-Bromo-2-chloro-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-3-methyl-3H-benzooxazol-2-oneHCID 66697011—

Reaktionsschritte

Trifluoromethyltrimethylsilane (2M in THF, 1.48 mL) was added at 0° C. to a solution of 6-[2-(4-bromo-2-chloro-phenyl)-propionyl]-3-methyl-3H-benzooxazol-2-one (531 mg) in THF (15 mL) followed by the addition of tetrabutylammonium fluoride trihydrate (424 mg). Stirring was continued for 48 hours at r.t. The reaction mixture was poured into ice/water and extracted two times with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent was evaporated. The residue was purified by flash chromatography (silica gel, heptane:ethyl acetate=7:3) to give the title compound as a orange amorphous foam (440 mg, 70%). MS (neg. ion, m/e)=464.0 [(M−H)−].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08450313B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-cc7d8695385e43a8ab60d5a58d207400
Quellennotizuspto-grants-2013_05