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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167181Generated: November 3, 2026

Imidazole → 2-phenyl-3-methyl-8-(1-(S)-hydroxy-2-[tert-butyldimethylsilyloxy]ethyl)quinoline

https://huagongshe.com/reaction/1167181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-phenyl-3-methyl-8-(1-(S),2-dihydroxyethyl)quinolineHCID 21356543—
SolventDimethylformamideHCID 6228—
Product2-phenyl-3-methyl-8-(1-(S)-hydroxy-2-[tert-butyldimethylsilyloxy]ethyl)quinolineHCID 2135654492%

Reaction Steps

3.7 g (24.3 mmol) of tert-butyldimethylsilyl chloride and 3.4 g of (50 mmol) of imidazole are added at ambient temperature to a solution of 6.5 g (23.2 mmol) of 2-phenyl-3-methyl-8-(1-(S),2-dihydroxyethyl)-quinoline in 200 ml of dimethylformamide. The reaction medium is stirred for 16 hours. After addition of 200 ml of distilled water, the reaction mixture is extracted with 3×200 ml of ethyl acetate. The organic phases are combined, washed with 300 ml of distilled water, dried over magnesium sulfate, filtered and concentrated under vacuum. The residue is purified by silica gel chromatography (eluent: ethyl acetate/cyclohexane to provide 8.4 g of 2-phenyl-3-methyl-8-(1-(S)-hydroxy-2-[tert-butyldimethylsilyloxy]ethyl)quinoline in the form of a colorless oil. (Yield: 85%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617336B1
Source datasetuspto-grants-2003_09
ORD IDord-4da1e5de9ba44f47ab078b4dd1d361bb
Source noteuspto-grants-2003_09