HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529422Generated: October 26, 2026
Acetic Acid → 2-(4-Bromophenoxy)-5-methoxynicotinic acid
https://huagongshe.com/reaction/529422
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Fluoro-5-methoxynicotinic acid | HCID 66728073 | — |
| Product | 2-(4-Bromophenoxy)-5-methoxynicotinic acid | HCID 66728166 | — |
Reaction Steps
To a slurry of sodium hydride (60% dispersion) (21.74 g, 543 mmol) in DMF (351 mL, 175 mmol) at 0° C. was added 4-bromophenol (60.7 g, 351 mmol) over the course of 5 minutes. Stirred at 0° C. for two minutes then removed from the ice bath and stirred for an additional 5 minutes at room temperature. Added 2-fluoro-5-methoxynicotinic acid (30 g, 175 mmol) portionwise over 10 minutes and heated the resulting slurry at 140° C. After cooling to RT the mixture was then poured onto 1 kg of ice and was quenched with acetic acid (50.2 mL, 877 mmol) and then 75 mL of 6 N HCl. Stirred vigorously for 1 hour, leading to the formation of a red slurry containing a very fine white precipitate. The slurry was filtered to provide 2-(4-bromophenoxy)-5-methoxynicotinic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346827B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8e0e3317982f44f6b660169ef17a8ce8 |
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| Source note | uspto-grants-2016_05 |
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