HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427451Generated: October 31, 2026
Ethyl Acetate → 3-Methyl-5-nitro-2-[4-(trifluoromethyl)phenyl]pyridine
https://huagongshe.com/reaction/1427451
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Trifluoromethyl)phenylboronic acid | HCID 2734389 | — |
| Reactant | 2-Bromo-3-methyl-5-nitropyridine | HCID 5200466 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Methyl-5-nitro-2-[4-(trifluoromethyl)phenyl]pyridine | HCID 67153433 | 79% |
Reaction Steps
To a mixture of 4-(trifluoromethyl)phenylboronic acid (285 mg, 1.5 mmol), 2-bromo-3-methyl-5-nitropyridine (216 mg, 1.0 mmol), and potassium carbonate (345 mg, 2.5 mmol) in water (1.5 mL) and dioxane (6 mL) was added tetrakis(triphenylphosphine)palladium(0) (40 mg, 0.035 mmol). The resulting mixture was stirred at 80° C. for 4.5 hours. The mixture was cooled to room temperature. Ethyl acetate was added and the mixture was washed with water, then brine, dried over sodium sulfate, filtered and concentrated. Purification by column chromatography gave 3-methyl-5-nitro-2-(4-(trifluoromethyl)phenyl)pyridine (223 mg, 79%). 1H NMR (400 MHz, CDCl3, δ): 9.35 (s, 1H), 8.42 (s, 1H), 7.77 (d, 2H), 7.69 (d, 2H), 2.51 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933104B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-8e96afd0e01c4b57b4e69d613eb426e9 |
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| Source note | uspto-grants-2015_01 |
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