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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535758Generated: October 30, 2026

Sodium hydride → HCID 67053515, compound

https://huagongshe.com/reaction/535758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
ReactantHCID 67053567HCID 67053567—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67053515HCID 6705351516.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 250 mL round-bottom flask was purged with nitrogen and charged with NaH (95%, 0.2 g, 8.3 mmol). THF (10 mL) added, and the mixture cooled to 0° C. After 5 minutes, a solution of 4,5-dibromo-2-cyclobutyl-1H-imidazole (1.76 g, 6.29 mmol, ˜40% purity) in THF (20 mL) was added dropwise from an addition funnel over 5 minutes. The reaction was stirred at 0° C. for 35 minutes and SEMCl (1.8 mL, 10.2 mmol) was then added dropwise over 2 minutes. After 5 minutes, ice bath was removed, and the reaction stirred at room temperature for 4 hours. LCMS indicated complete reaction. The reaction was then carefully quenched with water (1.5 mL). Heptane (250 mL) was added and organic layer was washed with water (200 mL). The aqueous layer was extracted with heptane (100 mL), and the combined organic layers were washed with water and brine, dried (Na2SO4), and concentrated to give 2.14 g of crude material. The crude material was purified by flash chromatography (SiO2; EtOAc in heptane) to afford 4,5-dibromo-2-cyclobutyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole (0.43 g) as a yellow oil: LCMS (m/z) 408.9 (MH+), tR=1.25 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859548B2
Source datasetuspto-grants-2014_10
ORD IDord-3f4b104273e34c0093f6a6dd9a9cb537
Source noteuspto-grants-2014_10