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Dimethylformamide → 4-methyl-1,5-octadiyn-4(RS)-ol triethylsilyl ether
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Chlorotriethylsilane | HCID 13819 | — |
| 反応物 | 4-methyl-1,5-octadiyn-4(RS)-ol | HCID 21322039 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-methyl-1,5-octadiyn-4(RS)-ol triethylsilyl ether | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04151187 |
| 出典データセット | uspto-grants-1979_04 |
| ORD ID | ord-689e2f5deb7742b2b55bcd01eb67d1b2 |
| 出典メモ | uspto-grants-1979_04 |