HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172293Generated: October 30, 2026
Potassium Carbonate → 4-(2-Bromo-5-(trifluoromethyl)phenyl)pyridine
https://huagongshe.com/reaction/2172293
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (Pyridin-4-yl)boronic acid | HCID 2734379 | — |
| Reactant | 1-Bromo-2-iodo-4-(trifluoromethyl)benzene | HCID 46735231 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(2-Bromo-5-(trifluoromethyl)phenyl)pyridine | HCID 86687340 | 41.4% |
Reaction Steps
A solution of pd(ph3p)4 (1.410 g, 1.220 mmol), 1-bromo-2-iodo-4-(trifluoromethyl)benzene (3.94 ml, 24.41 mmol), pyridin-4-ylboronic acid (3.00 g, 24.41 mmol), and potassium carbonate (13.49 g, 98 mmol) in 32 mL dioxane and 6 mL water was heated to 120° C. overnight. Additional portions of pyridin-4-ylboronic acid (3.00 g, 24.41 mmol) and potassium carbonate (13.49 g, 98 mmol) were added and the reaction mixture was heated to 120° C. for 3 hours. The reaction mixture was then poured into water and was extracted with DCM. The organics were then concentrated. Purification of the crude residue by silica gel column chromatography (0-100% EtOAc/heptane) gave 4-(2-bromo-5-(trifluoromethyl)phenyl)pyridine (3.054 g, 10.11 mmol, 41.4% yield) as a white solid. [M+H]+=303.9
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051311B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-0160cba926f14d01886ae1c13f15487d |
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| Source note | uspto-grants-2015_06 |
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