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HRID 26270作成日:2026年10月25日

Imidazole → Trimethyl[(2-methyl-1-phenoxybut-3-yn-2-yl)oxy]silane

https://huagongshe.com/reaction/26270

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物ChlorotrimethylsilaneHCID 6397—
反応物Diethylether waterHCID 21584184—
反応物2-Methyl-1-phenoxybut-3-yn-2-olHCID 23266458—
溶媒DimethylformamideHCID 6228—
生成物Trimethyl[(2-methyl-1-phenoxybut-3-yn-2-yl)oxy]silaneHCID 21325376—

反応手順

The hydroxyl group of this alkyne is protected by dissolving 2 parts of the butyne in 5 parts by volume of dimethylformamide and successively treating the reaction mixture with 2 parts of imidazole and 1.2 parts of trimethylsilylchloride. The reaction mixture is stirred at room temperature for 1 hour and poured into ether/water. The ethereal layer is washed with water and dried over anhydrous sodium sulfate. Isolation by low pressure liquid chromatography on silica gel provides 3-methyl-3-trimethylsilyloxy-4-phenoxy-1-butyne.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04149006
出典データセットuspto-grants-1979_04
ORD IDord-2d05f06d6e454e9bb29f86245611036f
出典メモuspto-grants-1979_04