HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178342Generated: October 29, 2026
Potassium Carbonate → 5-((4-Bromo-5-fluoro-2-methoxyphenoxy)methyl)-2-methoxypyridine
https://huagongshe.com/reaction/2178342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-5-fluoro-2-methoxyphenol | HCID 26596525 | — |
| Reactant | 5-(Chloromethyl)-2-methoxypyridine hydrochloride | HCID 53438957 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-((4-Bromo-5-fluoro-2-methoxyphenoxy)methyl)-2-methoxypyridine | HCID 118113980 | 66% |
Reaction Steps
To a stirred solution of 4-bromo-5-fluoro-2-methoxyphenol (2.82 g, 12.25 mmol) in N,N-dimethylformamide (50 mL) was added 5-(chloromethyl)-2-methoxypyridine hydrochloride (2.50 g, 12.86 mmol) and potassium carbonate (5.08 g, 36.75 mmol). The reaction mixture was heated to 100° C. After 2 h, the mixture was allowed to cool to room temperature and was diluted with water. The mixture was extracted with ethyl acetate (3×25 mL). The combined organic phases were washed with brine, dried over magnesium sulfate, filtered, and concentrated. Chromatographic purification (0-33% ethyl acetate/hexanes elute) afforded 2.76 g (66%) of 5-((4-bromo-5-fluoro-2-methoxyphenoxy)methyl)-2-methoxypyridine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09067914B1 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-84e4e516a7644a02ad5e2b2925c62aeb |
|---|
| Source note | uspto-grants-2015_06 |
|---|