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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627231Generated: November 1, 2026

Carbon Dioxide → HCID 58506078, compound

https://huagongshe.com/reaction/1627231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
Reactant2,4,5-tribromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-ImidazoleHCID 10906203—
ReactantHCID 178506676HCID 178506676—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58506078HCID 58506078—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2,4,5-tribromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole (5.0 g, 11.5 mmol) in tetrahydrofuran (200 ml) at −78° C. is added phenyl lithium (7.0 ml, 12.6 mmol, 1.8 M in THF). After 30 minutes stirring at −78° C. CO2-pellets (˜3.0 g) are added. The mixture is allowed to warm to room temperature, water is added, and the pH is carefully adjusted with 6N HCl (aqueous) to pH=5. The mixture is extracted with ethyl acetate (2×50 ml) and the combined organic layer is washed with brine, dried over MgSO4, filtered and evaporated in vacuo. The crude 4,5-dibromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid is obtained as a yellow oil, and used without further purification 4.2 g, 91%, LC/MS ESI m/z (M−H)−398.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785489B2
Source datasetuspto-grants-2014_07
ORD IDord-eb33cec02b5a4d4ba3ed0d63282034fd
Source noteuspto-grants-2014_07