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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640041Generated: November 3, 2026

Water → HCID 13081737, compound

https://huagongshe.com/reaction/1640041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-BromoquinolineHCID 21413—
ReactantTrimethylsilylacetyleneHCID 66111—
CatalystHCID 178418476HCID 178418476—
SolventDiethyl EtherHCID 3283—
ProductHCID 13081737HCID 13081737—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 3-bromoquinoline (10.40 g, 0.05 mol), trimethylsilylacetylene (8.48 mL, 0.06 mol), cuprous iodide (0.5 g) and trans-dichlorobis(triphenylphosphine)palladium (1 g) and TEA (15 mL) was heated at 70° C. in a sealed tube for 1 h. H2O (150 mL) was added, followed by Et2O (300 mL). The organic layer was separated and the aqueous layer extracted with Et2O (200 mL). The combined organic layers were dried (Na2SO4) and concentrated. The residue was purified by flash column chromatography (eluent: 100% DCM) to give 3-(trimethylsilylethynyl) quinoline as a brown oil. 3-(Trimethylsilylethynyl) quinoline was dissolved in anhydrous MeOH (100 mL) and K2CO3 (0.69 g, 5 mmol) was added. The mixture was stirred at rt for 1 h and DCM (250 mL) was added. The mixture was filtered over celite. The filtrate was evaporated and the residue was purified by flash column chromatography to give Compound 13b as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110683B2
Source datasetuspto-grants-2012_02
ORD IDord-cd97f229df134d3e807ca914ef989345
Source noteuspto-grants-2012_02