반응식
FC1C=C(CC=O)C=CC=1.FC1C=C(C=CC(C(C)C)C(OCC)=O)C=CC=1.[OH-].[K+].CO.O.[F:34][C:35]1[CH:36]=[C:37]([CH:41]=[CH:42][CH:43]([CH:47]([CH3:49])[CH3:48])[C:44]([OH:46])=[O:45])[CH:38]=[CH:39][CH:40]=1.[C:50]([CH:52](O)[C:53]1[CH:58]=[CH:57][CH:56]=[C:55]([O:59][C:60]2[CH:65]=[CH:64][CH:63]=[CH:62][CH:61]=2)[CH:54]=1)#[N:51]>>[F:34][C:35]1[CH:36]=[C:37]([CH:41]=[CH:42][CH:43]([CH:47]([CH3:49])[CH3:48])[C:44]([O:46][CH:52]([C:50]#[N:51])[C:53]2[CH:58]=[CH:57][CH:56]=[C:55]([O:59][C:60]3[CH:61]=[CH:62][CH:63]=[CH:64][CH:65]=3)[CH:54]=2)=[O:45])[CH:38]=[CH:39][CH:40]=1참가 물질
6
반응물 5
생성물 1
실험 절차
3-Fluorophenylacetaldehyde is converted into ethyl 4-(3-fluorophenyl)-2-isopropyl-3-butenoate using the reaction of Example 9. The ester is hydrolyzed using KOH/MeOH/H2O to 4-(3-fluorophenyl)-2-isopropyl-3-butenoic acid, which is converted to the acid chloride and reacted with α-cyano-m-phenoxybenzyl alcohol to yield α-cyano-m-phenoxybenzyl 4-(3-fluorophenyl)-2-isopropyl-3-butenoate, MS m/e 429 (M+).
후처리
- customthe reaction of Example 9
출처 및 근거
- ORD 기록
- ord-245c751cc7cd4033b3be1cd9c8f7ee54
- 출처 데이터셋
- uspto-grants-1980_05
- 특허 번호
- US04204071
연결된 노트
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