HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915645Generated: October 25, 2026
Hydrochloric Acid → 6-(4-Fluorophenyl)nicotinic acid
https://huagongshe.com/reaction/915645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-(4-Fluorophenyl)pyridine-3-carboxylic acid methyl ester | HCID 11031712 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(4-Fluorophenyl)nicotinic acid | HCID 22730186 | 37% |
Reaction Steps
Combine 6-bromopyridine-3-carboxylic acid methyl ester (1.03 g, 4.78 mmol), 4-fluorophenylboronic acid (1.88 g, 13.41 mmol), and cesium fluoride (2.55 g, 16.78 mmol) in dimethylformamide (25 mL) and water (4 mL) with stirring. Place the hetereogeneous reaction mixture, open to the air, in an oil bath maintained at 80° C. After 5 minutes of heating, add Pd(OAc)2 (150 mg, 0.67 mmol) in one portion. After 17 hours, cool the reaction to room temperature, dilute with ethyl acetate and filter through a short plug of celite with additional ethyl acetate. Wash the organics with water, dry over magnesium sulfate, filter and evaporate. Purification by flash column chromatography yields 6-(4-fluorophenyl)pyridine-3-carboxylic acid methyl ester as a yellow solid. Dissolve the purified ester in tetrahydrofuran (0.25M) and add an equal volume of 1M sodium hydroxide. Stir vigorously at room temperature for 15 hours. Upon completion, acidify the reaction with conc. HCl and collect the white precipitate by filtration. Drying under vacuum yields 385 mg (37%) of the title compound. MS (m/e): 218.1 (MH+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07265246B2 |
|---|
| Source dataset | uspto-grants-2007_09 |
|---|
| ORD ID | ord-b8cdfeb52b11472289bb9451a9088714 |
|---|
| Source note | uspto-grants-2007_09 |
|---|