Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diisobutylaluminumhydride → 9-(3',5'-Bistrifluoromethylbenzyloxy)nona-2-en-1-ol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diisobutylaluminumhydride | HCID 21225700 | — |
| 반응물 | Ethyl 9-(3',5'-bistrifluoromethylbenzyloxy)nona-2-enoate | HCID 54133067 | — |
| 용매 | Toluene methylene chloride | HCID 21877217 | — |
| 생성물 | 9-(3',5'-Bistrifluoromethylbenzyloxy)nona-2-en-1-ol | HCID 54143522 | 85.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05162367 |
| 출처 데이터셋 | uspto-grants-1992_11 |
| ORD ID | ord-e2e70361501e4fbabea613fdc2d41a7a |
| 출처 메모 | uspto-grants-1992_11 |