戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 551707作成日:2026年10月26日

2-({[Tert-butyl(dimethyl)silyl]oxy}methyl)butanal → Tert-butyl[(2-ethylbut-3-en-1-yl)oxy]dimethylsilane

https://huagongshe.com/reaction/551707

反応式

関与物質

役割名称HCID仕込み量
反応物2-({[Tert-butyl(dimethyl)silyl]oxy}methyl)butanalHCID 10846403—
反応物ButyllithiumHCID 178418339—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl[(2-ethylbut-3-en-1-yl)oxy]dimethylsilaneHCID 86646162—

反応条件

温度0 °C

反応手順

(Methyl)triphenylphosphonium bromide (59.1 g, 165 mmol) was suspended in tetrahydrofuran (330 mL). To the suspension, n-butyllithium (1.57 M hexane solution, 97.3 mL, 153 mmol) was gradually added with stirring at 0° C. The mixture was stirred at this temperature for 1 hour, and a tetrahydrofuran solution (110 mL) of 2-({[tert-butyl(dimethyl)silyl]oxy}methyl)butanal (Tetrahedron 2004, 60, 9307) (27.6 g, 127 mmol) was then gradually added thereto. The mixture was stirred at 0° C. for 2 hours, and the reaction was then terminated by the addition of a saturated aqueous solution of ammonium chloride and water, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of ammonium chloride, water, and saturated saline and then dried over anhydrous sodium sulfate. The residue was filtered and concentrated under reduced pressure. Then, the obtained crude product was purified by silica gel column chromatography to obtain the compound of interest as an oil substance (19.9 g, 73%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947738B2
出典データセットuspto-grants-2011_05
ORD IDord-36b39e91f59f450ab6c28f6a0d0bc785
出典メモuspto-grants-2011_05