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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400239Generated: October 30, 2026

Water → Ethyl 2-(2-phenyloxazol-4-yl)nicotinate

https://huagongshe.com/reaction/1400239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl chloronicotinateHCID 2796614—
Reactant2-Phenyl-1,3-oxazole-4-boronic acid, pinacol esterHCID 11558104—
CatalystHCID 178439029HCID 178439029—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-(2-phenyloxazol-4-yl)nicotinateHCID 6754058942%

Reaction Conditions

Temperature65 °C

Reaction Steps

[1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) dichloride (22 mg, 0.032 mmol) was added to a mixture of ethyl-2-chloronicotinate (120 mg, 0.647 mmol) and 2-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)oxazole (220 mg, 0.811 mmol) in dioxane (5 mL). After the addition of K2CO3 (402 mg, 2.910 mmol) the reaction mixture was heated at 65° C. for 4 h and then allowed to cool to room temperature. Water was added and the mixture was extracted with EtOAc. The combined organic layers were washed with water and dried (MgSO4). Purification of the thus obtained raw product by flash column chromatography (dichloromethane/EtOAc, gradient 5-10% EtOAc) provided the title compound (80 mg, 42%); ESI-MS [M+H+]=295.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906941B2
Source datasetuspto-grants-2014_12
ORD IDord-2f4f9d04cb6d4f4db6cd9ea6bbb516ca
Source noteuspto-grants-2014_12