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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
ReactantEthylacetate methanolHCID 21584119—
SolventTetrahydrofuranHCID 8028—
Product1-((2-(Trimethylsilyl)ethoxy)methyl)-1H-imidazoleHCID 1105260570%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772247B2
Source datasetuspto-grants-2010_08
ORD IDord-c09c286d156c44bdb3b4d7d1453c64da
Source noteuspto-grants-2010_08