HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539394Generated: October 31, 2026
Imidazole → 1-((2-(Trimethylsilyl)ethoxy)methyl)-1H-imidazole
https://huagongshe.com/reaction/539394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-((2-(Trimethylsilyl)ethoxy)methyl)-1H-imidazole | HCID 11052605 | 134.7% |
Reaction Steps
Under an argon atmosphere, a dimethylformamide (500 mL) suspension of sodium hydride (60%, 18.9 g) was ice-cooled and then imidazole (30.9 g) was added so as to prevent an inner temperature from rising to 5° C. or higher. The reaction solution was stirred at 0° C. for 45 minutes. To the reaction solution, 2-(trimethylsilyl)ethoxymethyl chloride (72.4 g) was added dropwise. The reaction solution was stirred at room temperature for 14 hours. To the reaction solution, ice water (200 mL) was added. The aqueous layer was extracted twice with a solution (n-hexane:ethyl acetate=1:1 (200 mL)). The combined organic layer was washed with saturated sodium chloride solution and then dried over anhydrous magnesium sulfate. After removing anhydrous magnesium sulfate by filtration, the filtrate was concentrated to obtain the title compound (116 g) having the following physical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871210B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-e4383b5c84144c13bec20ac4a4d1e79e |
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| Source note | uspto-grants-2014_10 |
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