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Tetrahydrofuran → 3,7,11-Trimethyl-12-(methoxymethyl)oxy-6,10-dodecadien-1-in-3-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 6,10-Dimethyl-11-(methoxymethyl)oxy-5,9-undecadien-2-one | HCID 54076998 | — |
| 生成物 | 3,7,11-Trimethyl-12-(methoxymethyl)oxy-6,10-dodecadien-1-in-3-ol | HCID 131718158 | 83% |
反応手順
A solution of 6,10-dimethyl-11-(methoxymethyl)oxy-5,9-undecadien-2-one (67 mg, 0.26 mmol) in tetrahydrofuran (2 ml) was stirred on an ice bath under argon atmosphere. To the solution was added lithium acetylide ethylenediamine complex (30 mg, 0.33 mmol), and the mixture was warmed to room temperature and stirred for 3 hours. After addition of saturated aqueous ammonium chloride (2 ml), the reaction mixture was extracted with ether. The extract was dried over Na2SO4 and evaporated in vacuo to remove the solvent to give a crude product, which was purified with silica gel column chromatography to obtain 3,7,11-trimethyl-12-(methoxymethyl)oxy-6,10-dodecadien-1-in-3-ol (61 mg, 83%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05324869 |
| 出典データセット | uspto-grants-1994_06 |
| ORD ID | ord-f0ce53628e6a4df382e1c0868ffb6319 |
| 出典メモ | uspto-grants-1994_06 |