Dichlorodimethylsilane → Chlorodimethyl(n-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indol-6-yl)silane
반응식
[Li]CCCC.CCCCCC.[CH3:12][N:13]1[C:21]2[C:16](=[CH:17][C:18]([O:22][CH3:23])=[CH:19][CH:20]=2)[C:15]2[C:24]3[C:29]([CH2:30][C:14]1=2)=[CH:28][CH:27]=[CH:26][CH:25]=3.N1C2C(C=CC3C=2C=C2C=3C=CC=C2)=CC=1.[Cl:47][Si:48](Cl)([CH3:50])[CH3:49]>C1COCC1>[Cl:47][Si:48]([CH3:50])([CH3:49])[CH:30]1[C:14]2[N:13]([CH3:12])[C:21]3[C:16]([C:15]=2[C:24]2[C:29]1=[CH:28][CH:27]=[CH:26][CH:25]=2)=[CH:17][C:18]([O:22][CH3:23])=[CH:19][CH:20]=3참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- -78 °C
실험 절차
3.4 mL of a 2.5 M solution of n-BuLi in hexane (8.50 mmol) were added dropwise to a solution of 2.22 g of N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indole, obtained as reported above, (Mw=249.32, purity 85.8%, 7.64 mmol; indenoindole: n-BuLi=1:1.1) in 50 mL of THF, previously cooled to −78° C. At the end of the addition, the brown solution was allowed to warm up to room temperature and stirred for 5 hours. Then it was cooled again to −78° C. and added dropwise to a solution of dichlorodimethylsilane (Mw=129.06, d=1.064, 0.92 mL, 7.64 mmol; indenoindole: Me2SiCl2=1:1) in 20 mL of THF, previously cooled to −78° C. At the end of the addition, the dark brown solution was allowed to warm up to room temperature and stirred overnight. The solvents were evaporated under reduced pressure to give the desired product, containing few by-products, in the form of a brown sticky solid; this product was used in the following step without further purification.
후처리
- customobtained
- additionAt the end of the addition
- temperatureto warm up to room temperature
- temperatureThen it was cooled again to −78° C.
- temperaturepreviously cooled to −78° C
- additionAt the end of the addition
- temperatureto warm up to room temperature
- stirringstirred overnight
- customThe solvents were evaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-9d14bcbd2f9441b0b3c7912e56b43b56
- 출처 데이터셋
- uspto-grants-2004_05
- 특허 번호
- US06730754B2
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