HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41138Generated: October 26, 2026
Imidazole → 3-(2-((Triisopropylsilyl)oxy)ethyl)benzaldehyde
https://huagongshe.com/reaction/41138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Triisopropylsilyl chloride | HCID 139400 | — |
| Reactant | 3-(2-Hydroxyethyl)benzaldehyde | HCID 18424732 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2-((Triisopropylsilyl)oxy)ethyl)benzaldehyde | HCID 54757655 | 96% |
Reaction Steps
Chlorotriisopropylsilane (0.640 g, 0.71 mL, 3.3 mmol) was added dropwise to a 0° C. cooled solution of 13 (0.450 g, 3.0 mmol) and 1H-imidazole (0.410 g, 6.0 mmol) in anhydrous N,N-dimethylformamide (10 mL). The reaction mixture was stirred at 0° C. for 3 h and then diluted with water. The resulting mixture was extracted with diethyl ether, and the combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was purified by silica gel column chromatography using ethyl acetate-hexanes 1:9 as eluent to furnish the desired compound as colorless oil. Yield: 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530520B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-012aadcc994d48c0a6ed9bc397ef13bb |
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| Source note | uspto-grants-2013_09 |
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