戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 373206作成日:2026年10月26日

Diisobutylaluminumhydride → 9-(3',5'-Bistrifluoromethylbenzyloxy)nona-2-en-1-ol

https://huagongshe.com/reaction/373206

反応式

関与物質

役割名称HCID仕込み量
反応物DiisobutylaluminumhydrideHCID 21225700—
反応物Ethyl 9-(3',5'-bistrifluoromethylbenzyloxy)nona-2-enoateHCID 54133067—
溶媒Toluene methylene chlorideHCID 21877217—
生成物9-(3',5'-Bistrifluoromethylbenzyloxy)nona-2-en-1-olHCID 5414352285.1%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05162367
出典データセットuspto-grants-1992_11
ORD IDord-e2e70361501e4fbabea613fdc2d41a7a
出典メモuspto-grants-1992_11