HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431877Generated: October 25, 2026
Potassium Carbonate → Methyl-3-bromo-5-(3-pyridyl)benzoate
https://huagongshe.com/reaction/431877
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(1,3,2-Dioxaborinan-2-yl)pyridine | HCID 4198005 | — |
| Reactant | Methyl 3-bromo-5-iodobenzoate | HCID 21942573 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl-3-bromo-5-(3-pyridyl)benzoate | HCID 21942604 | 67.6% |
Reaction Steps
To the solution of Methyl-3-bromo-5-iodobenzoate (2.00 g, 5.87 mmol) in toluene (50 ml) added Pyridine-3-boronic acid-1,3-propanediol ester (1.24 g, 7.63 mmol), potassium carbonate (8.11 g, 58.7 mmol) and tetrakis(triphenylphoshine)palladium (0) (0.34, 0.29 mmol), sequentially. The resulting brownish yellow reaction mixture was heated at 80° C. under argon for 10 h. The reaction mixture was cooled to room temperature, filtered through a pad of celite and concentrated in-vacuo. The residue was purified on silica gel using 3% methanol in dichloromethane to isolate Methyl-3-bromo-5-(3-pyridyl)benzoate (1.16 g, 67%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06660753B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-ed585bb9e9d04a2598d44a04ce25484b |
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| Source note | uspto-grants-2003_12 |
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