HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51468Generated: October 27, 2026
Imidazole → 4-(t-Butyldimethylsilyloxy)indole
https://huagongshe.com/reaction/51468
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 1H-indol-4-ol | HCID 75421 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(t-Butyldimethylsilyloxy)indole | HCID 11593976 | — |
Reaction Steps
Imidazole (15.3 g, 225 mmol) was added to a solution of 4-hydroxyindole (20 g, 150 mmol) in 300 mL of anhydrous methylene chloride at ambient temperature. The resulting mixture was treated with tert-butyldimethylsilyl chloride (25 g, 165 mmol). After stirring overnight at ambient temperature, the reaction mixture was poured into 300 mL of water. The layers were separated, and the aqueous phase was extracted with methylene (2×100 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to a black oil. The crude residue was purified on a Prep 500 (silica gel; 0% to 5% ethyl acetate/hexanes) to give the title compound as a light purple waxy solid in quantitative yield. MS (ion spray, NH4OAc) m/e [M+1]+ 248, [M−1]− 246.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713645B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-c200170422d64c2696370ce4df865310 |
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| Source note | uspto-grants-2004_03 |
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