Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640143Generated: October 26, 2026

Potassium Carbonate → 2-(4-Prop-2-ynyl-benzyloxy)-pyridine

https://huagongshe.com/reaction/640143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-(4-Chloromethyl-benzyloxy)-pyridineHCID 59255095—
ReactantHCID 178418443HCID 178418443—
Catalystcopper(I) bromideHCID 24593—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Prop-2-ynyl-benzyloxy)-pyridineHCID 59255311—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of trimethylsilyl acetylene (496 μL, 3.51 mmol) in tetrahydrofuran (15 mL) was added ethyl magnesium bromide (3 M diethyl ether solution, 1.09 mL, 3.28 mmol) under nitrogen atmosphere at room temperature, which was stirred for 30 minutes at 65° C. The reaction solution was cooled to room temperature, and copper (I) bromide (168 mg, 1.17 mmol) and 2-(4-chloromethyl-benzyloxy)-pyridine (548 mg, 2.34 mmol) manufactured in Manufacturing Example 30-1-1 were added thereto and stirred for 15 hours and 10 minutes at 65° C. The reaction solution was partitioned into saturated aqueous ammonium chloride solution and ethyl acetate at room temperature. The organic layer was washed with saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. To a solution of the resulting residue in methanol (5 mL) and tetrahydrofuran (10 mL) was added potassium carbonate (647 mg, 4.68 mmol), which was stirred for 3 hours and 25 minutes at room temperature. The reaction solution was partitioned into water and ethyl acetate at room temperature. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=20:1) to obtain a mixture of the title compound and 2-(4-chloromethyl-benzyloxy)-pyridine (448 mg, target purity 20%, 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-1fe5d559c76f41e6b71b0d26fa74a92f
Source noteuspto-grants-2010_04