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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189159Generated: October 30, 2026

2-Methylquinoline → 2-(4-Trimethylsilanyl-but-3-ynyl)-quinoline

https://huagongshe.com/reaction/1189159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylquinolineHCID 7060—
Reactant3-Bromo-1-(trimethylsilyl)-1-propyneHCID 642589—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Trimethylsilanyl-but-3-ynyl)-quinolineHCID 6659843864%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-Methyl-quinoline (0.28 mL, 2.09 mmol) was added dropwise to a solution of LDA (3.0 mL, 0.8 M in THF) in THF (3 mL) at −78° C. and the reaction mixture was stirred for 1 hour at −78° C. Then (3-bromo-prop-1-ynyl)-trimethyl-silane (0.39 mL, 2.51 mmol) was added to the reaction mixture, the solution was stirred for 18 hours at room temperature and was quenched with water. The aqueous phase was extracted with DCM. The organic phase was washed with water, dried over MgSO4, filtered and evaporated. The crude residue was purified by flash chromatography (cyclohexane/AcOEt 9:1) to yield 338 mg (1.33 mmol, 64%) of 2-(4-trimethylsilanyl-but-3-ynyl)-quinoline as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-6454f2626c284450a6dd623b40e419a5
Source noteuspto-grants-2014_03