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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470693Generated: October 26, 2026

Imidazole → HCID 178453986, compound

https://huagongshe.com/reaction/470693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant1,3-Dibromo-2-propanolHCID 7287—
ReactantSodium CarbonateHCID 10340—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
ReactantHCID 178419079HCID 178419079—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 178453986HCID 17845398632.1%

Reaction Steps

1,3-Dibromo-2-propanol (1.70 ml, 16.5 mmol) and sodium carbonate (15.9 g, 150 mmol) were added to an ethanol (300 ml) solution of tert-butyl(trans-4-aminocyclohexyl)carbamate (3.21 g, 15.0 mmol) and the resulting mixture was stirred under heating to reflux overnight. After cooling, insoluble matter was removed by filtration through celite and then the filtrate was concentrated under reduced pressure. The residue was diluted with water, followed by extraction with ethyl acetate. Then the organic layer was washed with brine. The organic layer was dried over anhydrous sodium sulfate and then the solvent was evaporated under reduced pressure. The residue was dissolved in N,N-dimethylformamide (15 ml) and imidazole (2.45 g, 36.0 mmol) and tert-butyldiphenylchlorosilane (4.29 ml, 16.5 mmol) were added under ice cooling. After stirring at room temperature for 1 hour, the reaction mixture was diluted with ethyl acetate and washed with water and brine in that order. The organic layer was dried over anhydrous magnesium sulfate, then the solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography [chloroform:methanol=10:0→10:1 (v/v)] to give 2.45 g (32%) of the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629133B2
Source datasetuspto-grants-2014_01
ORD IDord-86272ab71bb749b899e6c1fda16ec9e8
Source noteuspto-grants-2014_01