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HRID 275550作成日:2026年10月27日

Trimethylsilylacetylene → Diethyl trimethylsilylethynylphosphonite

https://huagongshe.com/reaction/275550

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilylacetyleneHCID 66111—
反応物Ethyl phosphorochloriditeHCID 68530—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Diethyl trimethylsilylethynylphosphoniteHCID 53804595—

反応条件

温度-20 °C

反応手順

n-Butyllithium (26.02 ml, 1.55M in hexane) was added dropwise over thirty minutes to a stirred solution of trimethylsilylacetylene (5.18 ml) in dry tetrahydrofuran (25 ml), whilst maintaining the temperature below -65° C. After twenty minutes, diethylchlorophosphite (4.71 ml) was added dropwise over twenty minutes, then stirring continued for a further ninety minutes at -65° C. The stirred mixture was allowed to warm to -20° C., quenched by dropwise addition of saturated ammonium chloride solution (10 ml), then allowed to reach room temperature, diluted with water (10 ml) and extracted with chloroform (4×25 ml). The extracts were dried over magnesium sulphate and evaporated under reduced pressure to give diethyl trimethylsilylethynylphosphonite as a brown oil (7.34 g, 83% pure by GC).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05393732
出典データセットuspto-grants-1995_02
ORD IDord-01b0f93d550c45e19bf61efdb1888782
出典メモuspto-grants-1995_02