Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | HCID 12137096 | HCID 12137096 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 60110695 | HCID 60110695 | 89% |
Reaction Steps
0.50 g (12.6 mmol) of 60% strength sodium hydride in paraffin oil is introduced under argon into 20 ml of THF at room temperature. A solution of 2.0 g (8.40 mmol) of 5-bromo-3-isopropyl-1H-indole (Example X) in 20 ml of THF is added dropwise and the mixture is stirred until evolution of gas can no longer be detected. 2.03 g (13.44 mmol) of tert-butyl(chloro)dimethylsilane are subsequently added dropwise. After a short reaction time a precipitate deposits. The batch is stirred for 3 h at room temperature. It is treated with 200 ml of water. The aqueous phase is extracted twice with ethyl acetate, and the combined org. phases are dried and concentrated in a rotary evaporator. The residue is chromatographed on silica gel (eluent: cyclohexane). 2.63 g (89%) of 5-bromo-1-[tert-butyl(dimethyl)silyl]-3-isopropyl-1H-indole are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06794406B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-ad22692dd0244d419999decda45f115d |
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| Source note | uspto-grants-2004_09 |
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