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HRID 26665作成日:2026年10月26日

Dimethylformamide → 4-methyl-1,5-octadiyn-4(RS)-ol triethylsilyl ether

https://huagongshe.com/reaction/26665

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物ChlorotriethylsilaneHCID 13819—
反応物4-methyl-1,5-octadiyn-4(RS)-olHCID 21322039—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
生成物4-methyl-1,5-octadiyn-4(RS)-ol triethylsilyl etherHCID 21322041—

反応手順

A mixture consisting of 1.25 parts of 4-methyl-1,5-octadiyn-4(RS)-ol, 1.5 parts of triethylsilyl chloride, 2.5 parts by volume of dimethylformamide and 1 part by volume of triethylamine was stirred in an atmosphere of nitrogen at room temperature for about 24 hours. The mixture was then poured into benzene and diluted with water. The layers were separated and the organic layer was washed successively with dilute hydrochloric acid, water and saturated aqueous potassium bicarbonate, dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. Adsorption of the residue on a silica gel chromatographic column followed by elution with hexane afforded 4-methyl-1,5-octadiyn-4(RS)-ol triethylsilyl ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04151187
出典データセットuspto-grants-1979_04
ORD IDord-689e2f5deb7742b2b55bcd01eb67d1b2
出典メモuspto-grants-1979_04