HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420721Generated: October 30, 2026
Potassium Carbonate → 5-Bromo-6-methylpyridine-3-carbaldehyde
https://huagongshe.com/reaction/420721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trimethylboroxine | HCID 574072 | — |
| Reactant | Methyl 5-broMo-6-iodonicotinate | HCID 58001714 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Bromo-6-methylpyridine-3-carbaldehyde | HCID 53485163 | 55.2% |
Reaction Steps
To a mixture of methyl 5-bromo-6-iodo-3-pyridinecarboxylate (232 mg, 0.679 mmol), tetrakis(triphenylphosphine)palladium (0) (39.2 mg, 0.034 mmol), and K2CO3 (281 mg, 2.036 mmol) in dioxane (5 ml), trimethylboroxin (0.095 ml, 0.679 mmol) was added under N2. The reaction mixture was heated at 110° C. and more tetrakis(triphenylphosphine)palladium (0) was added in several portions until starting material was not detected by HPLC. The reaction mixture was diluted with water and extracted three times with EtOAc. The combined organic phases were washed with brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude of reaction was purified by flash chromatography using Flashmaster II, a 5 g silica gel cartridge, and mixtures of hexane and EtOAc to afford the title compound (75 mg, 48%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08097628B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-f2aa4450e4574b9cbd11d4253020670d |
|---|
| Source note | uspto-grants-2012_01 |
|---|