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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115186Generated: October 30, 2026

Imidazole → 3-[5-(tert-Butyl-dimethyl-silanyloxy)-5-phenyl-pentanoyl]-4-phenyl-oxazolidin-2-on

https://huagongshe.com/reaction/2115186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-(5-Hydroxy-5-phenylpentanoyl)-4-phenyl-1,3-oxazolidin-2-oneHCID 18374581—
SolventDimethylformamideHCID 6228—
Product3-[5-(tert-Butyl-dimethyl-silanyloxy)-5-phenyl-pentanoyl]-4-phenyl-oxazolidin-2-onHCID 21083181—

Reaction Steps

30 g of 3-(5-Hydroxy-5-phenyl-pentanoyl)-4-phenyl-oxazolidin-2-on are solved in 50 ml of DMF. After addition of 14.3 g of imidazol and 19 g of tert. -Butyl-dimethylsilylchlorid in 25 ml of DMF the reaction is stirred at room temperature until all components are dissolved (2-4 h). The reaction solution is evaporated, and after water was added extracted by acetic acid ethylester. After drying of the organic phase by magnesium sulfate and evaporation compound I (product 1) is obtained: C26H35NO4Si (453.6) MS (ESI+) 476 (M+Na+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435727B2
Source datasetuspto-grants-2008_10
ORD IDord-7633d3e866844b62add08276df2edb54
Source noteuspto-grants-2008_10