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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl chloronicotinate | HCID 2796614 | — |
| Reactant | 2-Phenyl-1,3-oxazole-4-boronic acid, pinacol ester | HCID 11558104 | — |
| Catalyst | HCID 178439029 | HCID 178439029 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 2-(2-phenyloxazol-4-yl)nicotinate | HCID 67540589 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906941B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-2f4f9d04cb6d4f4db6cd9ea6bbb516ca |
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| Source note | uspto-grants-2014_12 |
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