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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860724Generated: October 26, 2026

Dichloromethane → 2,4,5-tribromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-Imidazole

https://huagongshe.com/reaction/860724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4,5-TribromoimidazoleHCID 16253—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
SolventDimethylformamideHCID 6228—
Product2,4,5-tribromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-ImidazoleHCID 1090620383%

Reaction Steps

To a solution of 2,4,5-tribromoimidazole (3.05 g, 10 mmol) in anhydrous DMF (50 mL) was added powdered K2CO3 (19 g, 137 mmol), and the resulting suspension was stirred vigorously and treated dropwise with SEMCl (2.3 g, 13.8 mmol). The suspension was then stirred vigorously overnight. The solid was filtered off and washed with fresh DMF (20 mL). The combined filtrates were then evaporated under reduced pressure. Methylene chloride (30 mL) was then added and the solution washed with 0.1 N Na2CO3 (3×50 mL), dried (Na2SO4), filtered and evaporated to give a residue, which was passed through a silica gel pad (CH2Cl2) and evaporated to give 3.6 g (83%) of the title compound as a colorless oil. 1H NMR (500 MHz, CDCl3) δ 0.01 (s, 9H), 0.93 (t, 2H, J=8.0 Hz), 3.60 (t, 2H, J=8.0 Hz), 5.32 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153848B2
Source datasetuspto-grants-2006_12
ORD IDord-bc1318da3dad48eb8677beeb40b2f4ac
Source noteuspto-grants-2006_12