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Diisobutylaluminumhydride → 9-(3',5'-Bistrifluoromethylbenzyloxy)nona-2-en-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisobutylaluminumhydride | HCID 21225700 | — |
| 反応物 | Ethyl 9-(3',5'-bistrifluoromethylbenzyloxy)nona-2-enoate | HCID 54133067 | — |
| 溶媒 | Toluene methylene chloride | HCID 21877217 | — |
| 生成物 | 9-(3',5'-Bistrifluoromethylbenzyloxy)nona-2-en-1-ol | HCID 54143522 | 85.1% |
反応手順
7-(3',5'-bistrifluoromethylbenzyloxy)heptan-1-al (See Example 2, 4.97g, 13.96 mmol) was reacted with carboethoxymethylene triphenylphosphorane (4.86g, 13.96 mmol, Lancaster Synthesis Ltd., U.K.) in dry dichloromethane to give ethyl 9-(3',5'-bistrifluoromethylbenzyloxy)nona-2- enoate (5g). The ester (5g, 13.55 mmol) was reacted with diisobutylaluminium hydride (27 mmol) in toluene-dichloromethane at -30°. After conventional work-up, 9-(3',5'-bistrifluoromethylbenzyloxy)nona-2-en-1-ol (4.43g) was obtained. The alcohol was converted into 9-(3',5'-bistrifluoromethylbenzyloxy)nona-2-en-al by Swern oxidation (oxalyl chloride-dimethylsulphoxide, see EP-A-164 187).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05162367 |
| 出典データセット | uspto-grants-1992_11 |
| ORD ID | ord-e2e70361501e4fbabea613fdc2d41a7a |
| 出典メモ | uspto-grants-1992_11 |