HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500796Generated: October 30, 2026
Imidazole → 1-((2-(Trimethylsilyl)ethoxy)methyl)-1H-imidazole
https://huagongshe.com/reaction/500796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| Reactant | Ethylacetate methanol | HCID 21584119 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-((2-(Trimethylsilyl)ethoxy)methyl)-1H-imidazole | HCID 11052605 | 70% |
Reaction Steps
To a stirred suspension of NaH (60% dispersion in oil, 0.65 g, 16.2 mmol) at 0° C. was added imidazole (1 g, 14.7 mmol) in THF (14 mL). The mixture was warmed to room temperature over 30 min, then re-cooled to 0° C. followed by an addition of (2-(chloromethoxy)ethyl)trimethylsilane (2.73 ml, 15.4 mmol). The combined mixture was warmed to room temperature over 1 h, quenched with saturated aqueous ammonium chloride, concentrated to dryness and partitioned between water and EtOAc. Organic phase was collected, dried over anhydrous sodium sulfate, filtered and evaporated. The residue was purified by column chromatography (eluents EtOAc, then MeOH/EtOAc 20:80), to afford the title compound (2.04 g, 70% yield) as a white solid. MS (m/z) 199.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772247B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-c09c286d156c44bdb3b4d7d1453c64da |
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| Source note | uspto-grants-2010_08 |
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