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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106834Generated: October 30, 2026

Triethylamine → Tert-butyl 4-[2-(4-(2-phenylethenyl)-3-pyridyl)ethynyl]benzoate

https://huagongshe.com/reaction/1106834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 4-ethynylbenzoateHCID 13965008—
Reactant3-Bromo-4-(2-phenylethenyl)pyridineHCID 53931587—
CatalystHCID 178506583HCID 178506583—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-[2-(4-(2-phenylethenyl)-3-pyridyl)ethynyl]benzoateHCID 5401687833%

Reaction Conditions

Temperature95 °C

Reaction Steps

3-Bromo-4-(2-phenylethenyl)pyridine (0.74 g, 2.9 mmol) was dissolved in DMF (1.4 ml). The solution was treated with tert-butyl 4-ethynylbenzoate (0.93 g, 4.6 mmol), copper (III) iodide (0.023 g, 0.21 mmol) and triethylamine (0.64 g, 6.3 mmol). The reaction mixture was degassed by bubbling through argon and the catalyst, bistriphenyl phosphinepalladium dichloride (0.03 g, 0.043 mmol), was added. The reaction was heated to 90-100° C. for 3 hours and then partitioned between ethyl acetate and water. The organic layer was washed with water (3×), dried (MgSO4) and evaporated. The residue was purified by chromatography (eluting with ethylacetate/hexane) to give tert-butyl 4-[2-(4-(2-phenylethenyl)-3-pyridyl)ethynyl]benzoate as a dark oil (0.36 g, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057345
Source datasetuspto-grants-2000_05
ORD IDord-75a8a525e6174f8c9d0c05e1e0adb425
Source noteuspto-grants-2000_05