반응식
[N+](=CC([O-])=O)=[N-].[Br:7][C:8]1[CH:13]=[CH:12][C:11]([C@@H:14]2[CH2:16][C@H:15]2[C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:10][CH:9]=1.BrC1C=CC(C=C)=CC=1.[Li+].[OH-]>>[Br:7][C:8]1[CH:9]=[CH:10][C:11]([C@@H:14]2[CH2:16][C@H:15]2[C:17]([OH:19])=[O:18])=[CH:12][CH:13]=1.[Br:7][C:8]1[CH:9]=[CH:10][C:11]([C@H:14]2[CH2:16][C@H:15]2[C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:12][CH:13]=1참가 물질
6
실험 절차
Another alternative is an enantioselective cyclopropanation using for example a bis-oxazoline chiral ligand/copper complex and diazoacetate (Evans et al. J. Am. Chem. Soc. 1991, 113, 726) to prepare optically active ethyl 2-(trans)-(4-bromophenyl)cyclopropanecarboxylate from 4-bromostyrene. Selective hydrolysis of the mixture of cis and trans isomer with LiOH (1 eq based on the trans ester) gave 2-(trans)-(4-bromophenyl)cyclopropanecarboxylic acid and ethyl 2-(cis)-(4-bromophenyl)cyclopropanecarboxylate which can be used in EXAMPLE 8.
후처리
- customhydrolysis of the mixture of cis and trans
출처 및 근거
- ORD 기록
- ord-3304206f5dce4347b5e856e4819413d0
- 출처 데이터셋
- uspto-grants-2007_07
- 특허 번호
- US07238706B2
연결된 노트
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