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HRID 2264285作成日:2026年10月25日

Triethylamine → Triisopropyl{[4-(2,4,5-trifluorophenyl)cyclohex-1-en-1-yl]oxy}silane

https://huagongshe.com/reaction/2264285

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ammonium ChlorideHCID 25517—
反応物Triisopropylsilyl trifluoromethanesulfonateHCID 2724529—
反応物4-(2,4,5-Trifluorophenyl)cyclohexanoneHCID 57424362—
溶媒DichloromethaneHCID 6344—
生成物Triisopropyl{[4-(2,4,5-trifluorophenyl)cyclohex-1-en-1-yl]oxy}silaneHCID 67065786—

反応条件

温度0 °C

反応手順

A three-neck flask (1 L) containing a stirred solution of 4-(2,4,5-trifluorophenyl)cyclohexanone (15.8 g) in dichloromethane (160 mL) under a nitrogen atmosphere was cooled to 0° C. and then treated with triethylamine (22 mL) followed by triisopropylsilyl trifluoromethanesulfonate (25.4 g) while maintaining the temperature below 5° C. The solution was stirred at 0° for 30 min and then allowed to rise to ambient temperature over a period of 0.5 h. It was then treated with saturated aqueous ammonium chloride solution. The organic layer was separated, dried over anhydrous magnesium sulfate and evaporated. The crude product was chromatographed (silica gel, 3% ether in hexane) to yield the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07855206B2
出典データセットuspto-grants-2010_12
ORD IDord-73796fe077a94abb8e44de766e7bcc96
出典メモuspto-grants-2010_12