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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401790Generated: October 31, 2026

Sodium hydride → 2,4-dibromo-5-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)thiazole

https://huagongshe.com/reaction/2401790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactant2,4-dibromo-5-(1H-imidazol-2-yl)thiazoleHCID 58094875—
SolventTetrahydrofuranHCID 8028—
Product2,4-dibromo-5-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)thiazoleHCID 5809476081.6%

Reaction Steps

To a mixture of sodium hydride (2.89 g, 72.2 mmol) in THF (431 mL) was added 2,4-dibromo-5-(1H-imidazol-2-yl)thiazole (18.8 g, 60.9 mmol) in THF (60 mL) at 0° C. After stirring 30 min, 2-(trimethylsilyl)ethoxymethyl chloride (11.8 mL, 66.9 mmol) in THF (24 mL) was slowly added at 0° C. After 30 min at this temperature, the reaction was quenched by the addition of MeOH (20 mL). The solvent was evaporated and the residue was purified by column chromatography on silica gel (0 to 25% EtOAc in hexanes). Product was obtained as colorless oil (21.8 g, 81.6%). LCMS: (AA) ES+, 440, 442. 1H NMR (300 MHz, CDCl3) δ: 7.24 (dd, 2H), 5.27 (s, 2H), 3.39 (t, 2H), 0.85 (t, 2H), −0.03 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796268B2
Source datasetuspto-grants-2014_08
ORD IDord-485bc71da5ed49f2ad09a999e583befc
Source noteuspto-grants-2014_08