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HRID 2096833作成日:2026年10月27日

(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

反応式

関与物質

役割名称HCID仕込み量
反応物(Trifluoromethyl)trimethylsilaneHCID 552549—
反応物Tetrabutylammonium Fluoride TrihydrateHCID 11726816—
反応物6-[2-(4-Bromo-2-chloro-phenyl)-propionyl]-3-methyl-3H-benzooxazol-2-oneHCID 66697107—
溶媒TetrahydrofuranHCID 8028—
生成物6-[2-(4-Bromo-2-chloro-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-3-methyl-3H-benzooxazol-2-oneHCID 66697011—

反応手順

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)−].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08450313B2
出典データセットuspto-grants-2013_05
ORD IDord-cc7d8695385e43a8ab60d5a58d207400
出典メモuspto-grants-2013_05