참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Indole | HCID 798 | — |
| 반응물 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane pyridine | HCID 19761730 | — |
| 생성물 | 1H-Indole, 3-bromo-1-[(1,1-dimethylethyl)dimethylsilyl]- | HCID 10244875 | 80.6% |
반응 단계
To a cold (-78°) solution of indole (4.0 g, 34 mmol) in THF (120 mL) was added nBuLi (2.5M/Hexanes) over 5 minutes. The solution was warmed to -10° (ice/salt bath) for 15 minutes, re-cooled to -78° and TBDMS-Cl (5.8 g, 38 mmol) was added in THF (30 mL). The solution was held at 0° for 3 hours, cooled to -78° and N-Bromosuccinimide (6.0 g, 34 mmol) was added in one portion. The solution was stirred coldfor 2 hours and then was allowed to warm to ambient temperature at which time hexane/pyridine (100 mL) was added to the solution and the resulting suspension was filtered over Celite. The organics were evaporated and the residue quickly purified by flash chromatography (hexanes/methylene chloride 2:1) giving 8.5 g of the desired compound as a slightly purple solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05952320 |
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| 출처 데이터셋 | uspto-grants-1999_09 |
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| ORD ID | ord-405b71d3674d4db98015a12cf13a547a |
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| 출처 메모 | uspto-grants-1999_09 |
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