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Diethyl Ether → (e)-7-(5-Bromo-2-thienyl)-3-ethyloct-6-en-3-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Ethyl (e)-5-(5-bromo-2-thienyl)-4-hexenoate | HCID 131724374 | — |
| 反応物 | HCID 178461633 | HCID 178461633 | — |
| 生成物 | (e)-7-(5-Bromo-2-thienyl)-3-ethyloct-6-en-3-ol | HCID 17934786 | — |
反応手順
3.3 g of ethyl (E)-5-(5-bromo-2-thienyl)-4-hexenoate (10.9 mmol) are dissolved in 50 mL of ethyl ether. 22 mL of 2.0 M ethylmagnesium chloride solution (44 mmol) are then added dropwise and the reaction medium is stirred at room temperature for 30 minutes. After treatment with saturated ammonium chloride solution, extraction with ethyl ether and then drying and evaporation of the solvents from the organic phase, the residue obtained is purified by chromatography on a column of silica. A colourless oil is obtained (m=2.4 g; Y=70%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06706725B1 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-9cabcb9eaaea42339cb7cae831b09958 |
| 出典メモ | uspto-grants-2004_03 |