반응식
[Li][CH2:2][CH2:3][CH2:4][CH3:5].[CH3:6][C:7]1[CH:15]=[CH:14][C:13]([CH3:16])=[C:12]2[C:8]=1[CH:9]=[CH:10][CH2:11]2.O>CCCCCC.C1COCC1.CCCCCC>[CH3:5][C:4]1[CH:11]=[CH:12][C:13]([CH3:16])=[C:2]2[C:3]=1[CH:2]=[CH:3][CH:4]2[C:5]1[CH:14]=[CH:15][CH:7]=[CH:8][C:9]=1[CH2:10][CH:11]1[C:12]2[C:8](=[C:7]([CH3:6])[CH:15]=[CH:14][C:13]=2[CH3:16])[CH:9]=[CH:10]1참가 물질
반응 조건
- 온도
- -70 °C
실험 절차
4.12 ml (10.3 mmoles) of n-BuLi 2.5 M in hexane are added to a solution of 1.48 g of 4,7-dimethyl indene (XVIII) (10.3 mmoles; obtained as described above) in 55 ml of a mixture of THF-hexane 2/1. At the end of the addition, the mixture is left under stirring for 1 hour. It is then cooled to −70° C. and a solution of 2.3 g of the brominated compound having formula (XX) (7.37 mmoles) in THF/hexane are added dropwise. The mixture is left to rise to room temperature and is left to rest for 6 hours. It is then poured into water and is extracted with ethyl ether. The organic phase is washed until neutrality and dehydrated on sodium sulfate. The residue obtained by evaporation of the solvent is purified by silica gel chromatography eluating with petroleum ether. After evaporation of the eluant 2.0 g of the bis-indenyl ligand having formula (XXI) and indicated below, are obtained (72% yield).
후처리
- additionAt the end of the addition
- waitthe mixture is left
- additionare added dropwise
- waitThe mixture is left
- customto rise to room temperature
- waitis left
- waitto rest for 6 hours
- extractionis extracted with ethyl ether
- washThe organic phase is washed until neutrality
- customThe residue obtained by evaporation of the solvent
- customis purified by silica gel chromatography
- customAfter evaporation of the eluant 2.0 g of the bis-indenyl ligand
- customare obtained (72% yield)
출처 및 근거
- ORD 기록
- ord-5126c223f2b14f7bab136e8816d4a689
- 출처 데이터셋
- uspto-grants-2001_04
- 특허 번호
- US06211110B1
연결된 노트
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