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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 373206생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/373206

반응식

참여 물질

역할이름HCID투입량
반응물DiisobutylaluminumhydrideHCID 21225700—
반응물Ethyl 9-(3',5'-bistrifluoromethylbenzyloxy)nona-2-enoateHCID 54133067—
용매Toluene methylene chlorideHCID 21877217—
생성물9-(3',5'-Bistrifluoromethylbenzyloxy)nona-2-en-1-olHCID 5414352285.1%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05162367
출처 데이터셋uspto-grants-1992_11
ORD IDord-e2e70361501e4fbabea613fdc2d41a7a
출처 메모uspto-grants-1992_11