HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175215Generated: November 3, 2026
Trifluoroacetic acid → HCID 68688990, compound
https://huagongshe.com/reaction/1175215
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-(Tributylstannyl)pyridine | HCID 607784 | — |
| Reactant | Methyl 3-bromo-2-fluorobenzoate | HCID 21584505 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68687070 | HCID 68687070 | 17% |
| Product | HCID 68688990 | HCID 68688990 | 23% |
Reaction Steps
In a 150 mL round bottom flask was combined methyl 3-bromo-2-fluorobenzoate (1.47 g, 6.3 mmol), DMF (10 mL), silver oxide (0.79 g, 6.4 mmol), 2-(tributylstannyl)pyridine (2.40 ml, 7.2 mmol), and dichlorobis(triphenylphosphine)-palladium (II) (0.23 g, 0.33 mmol) and the mixture was stirred at 100° C. to about 72 h. Monitoring the reaction by LC-MS revealed two products, the ester and the hydrolyzed product. The reaction was cooled, filtered through a pad of celite and the celite was washed with EtOAc. The filtrate was concentrated in vacuo and taken up in a small amount of DMF. The solution was purified by reverse-phase preparative HPLC on a Phenomenex Luna column (10 micron, C18, 100 Å, 150×50 mm) eluting at 45 ml/min with an linear gradient of 10% (v/v) to 100% MeCN (0.1% v/v TFA) in water (0.1% TFA) over 10 minutes to give 2-fluoro-3-(pyridine-2-yl)benzoic acid (0.24 g, 0.72 mmol, 23% yield) as a light red-colored TFA salt and methyl 2-fluoro-3-(pyridine-2-yl)benzoate (0.19 g, 0.55 mmol, 17% yield) as a golden syrup-colored TFA salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838676B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-f44e93f7190f4b1b9a8396872c2f9359 |
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| Source note | uspto-grants-2010_11 |
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