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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483172Generated: November 1, 2026

Imidazole → HCID 86727233, compound

https://huagongshe.com/reaction/1483172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(5S)-5-(hydroxymethyl)-1,3-oxazolidin-2-oneHCID 2793787—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86727233HCID 8672723383%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-5-(hydroxylmethyl)oxazolidin-2-one (1.61 g, 13.7 mmol) was dissolved in dried N,N-dimethyl formamide. Imidazole (1.87 g, 27.4 mmol) and DMAP (168 mg, 1.37 mmol) were added. The resulting mixture was cooled to 0° C., and then tert-butyldiphenylchlorosilane (5.66 g, 20.6 mmol) was added. The mixture was raised to room temperature to react for 4 hrs. The reaction was measured by TLC. After the reaction completed, the mixture was diluted with water, and extracted with ethyl acetate. The organic phase was combined, washed sequentially with water and saturated saline solution, dried over anhydrous sodium sulfate, and filtered. Column chromatography afforded 3.85 g of white solid (compound 25a), yield 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416144B2
Source datasetuspto-grants-2016_08
ORD IDord-0df0c243df58487e94804e3bbde28bf3
Source noteuspto-grants-2016_08