HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454061Generated: October 30, 2026
5-Bromoindole → 5-Bromo-1-(triisopropylsilyl)-1H-indole
https://huagongshe.com/reaction/1454061
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromoindole | HCID 24905 | — |
| Reactant | Triisopropylsilyl chloride | HCID 139400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-1-(triisopropylsilyl)-1H-indole | HCID 2794652 | 96% |
Reaction Steps
5-Bromoindole (2.5 g, 12.75 mmol) was dissolved in tetrahydro ran (THF; 50 mL) and cooled to 0° C. and Sodium Hydride NaH (920 mg, 23 mmol, 60%) was added in portions. The mixture was allowed to warm to RT with stirring for 1 hour. The reaction mixture was again cooled to 0° C. and triisopropylsilyl chloride (TIPSCl; 2.78 mL, 13.1 mmol) was added dropwise. The mixture was allowed to warm to room temperature and was stirred overnight. The mixture was washed with 2.0 N H3PO4, and the organic layer was dried over MgSO4, filtered and evaporated. The residue was purified by flash silica chromatography (100% Hexanes) to give compound 8 as an oil (4.3 g; 96% yield; M+1=353.4)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476746B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-7ec3742ea0424b58bf577ef295670832 |
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| Source note | uspto-grants-2009_01 |
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