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HRID 40281作成日:2026年10月24日

(Trifluoromethyl)trimethylsilane → (R)-N-((S)-1-(4-bromo-2-chlorophenyl)-2,2,2-trifluoroethyl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/ja/reaction/40281

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(NZ,R)-N-[(4-bromo-2-chlorophenyl)methylidene]-2-methylpropane-2-sulfinamideHCID 57691068—
溶媒DimethylformamideHCID 6228—
生成物(R)-N-((S)-1-(4-bromo-2-chlorophenyl)-2,2,2-trifluoroethyl)-2-methylpropane-2-sulfinamideHCID 57691004—

反応条件

温度35 °C

反応手順

To a stirring solution of (R,Z)—N-(4-bromo-2-chlorobenzylidene)-2-methylpropane-2-sulfinamide (1370 mg, 4246 μmol) and (trifluoromethyl)trimethylsilane (943 μl, 6369 μmol) in DMF (5 mL) was added 1,3-bis(1-adamantyl)imidazol-2-ylidene (143 mg, 425 μmol). Reaction stirred at 35° C. for 18 h then quenched with sat NH4Cl (10 mL). Reaction partitioned between EtOAc (40 mL) and 5% NaHCO3 (10 mL). Organic dried over MgSO4, concentrated to and oil from toluene, then purified on silica (80 g) eluting with 20>30% EtOAc/Hex. Product isolated as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524900B2
出典データセットuspto-grants-2013_09
ORD IDord-84a8c92d8359439a826c6de7927ce471
出典メモuspto-grants-2013_09