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HRID 1454783作成日:2026年10月26日

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

https://huagongshe.com/reaction/1454783

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US07482336B2
出典データセットuspto-grants-2009_01
ORD IDord-d7ac397f1cff4f2bbf658c7775a95694
出典メモuspto-grants-2009_01