化工社化工社 化学情報印刷レポート · 研究参考用
Hydrochloric Acid → (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienal
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 3-Nitrobenzaldehyde | HCID 7449 | — |
| 反応物 | Aluminum isopropoxide | HCID 11143 | — |
| 反応物 | Farnesol | HCID 445070 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 生成物 | (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienal | HCID 5280598 | 96% |
反応手順
(2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol (445 mg, 2.0 mmol) was dissolved in cyclohexane (1 mL), added with aluminum isopropoxide (40 mg, 0.1 eq, 0.2 mmol) and 3-nitrobenzaldehyde (393 mg, 1.3 eq, 2.6 mmol) and stirred at room temperature for 2 hours. The reaction mixture was added with hexane, then made acidic with addition of 1 N hydrochloric acid and extracted twice with ethyl acetate. Subsequently, the organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated in vacuo, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) to obtain 427 mg (yield: 96%, E:Z=99:1) of the title compound as yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06703527B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-e95a46d4355c47f6afb7014336a8dda3 |
| 出典メモ | uspto-grants-2004_03 |