HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293265Generated: November 1, 2026
Tetrafluoroboric acid → Methyl 5-chloro-2-[(5-fluoropyridin-2-yl)oxy]benzoate
https://huagongshe.com/reaction/1293265
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | Methyl 2-[(5-aminopyridin-2-yl)oxy]-5-chlorobenzoate | HCID 69415937 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 5-chloro-2-[(5-fluoropyridin-2-yl)oxy]benzoate | HCID 69418811 | 42% |
Reaction Steps
To a solution of sodium nitrite (224 mg, 3.25 mmol) in water (5 mL) was added methyl 2-[(5-aminopyridin-2-yl)oxy]-5-chlorobenzoate (907 mg, 3.25 mmol) and 48% tetrafluoroboric acid in water (5 mL) at 0° C. The reaction mixture was stirred for 5 h. The resulting precipitate was collected by filtration and dried under reduced pressure at room temperature. To the solids of tetrafluoroborate were added chlorobenzene (5 mL) and the mixture was heated at 140° C. for 40 min. The reaction mixture was diluted with ethyl acetate. The solution was washed with brine and concentrated. The residue was purified by flush column chromatography on silica gel eluting with hexane/ethyl acetate (8/1) to afford 382 mg (42%) of the title compound: 1H-NMR (CDCl3) δ 7.98 (1H, d, J=2.8 Hz), 7.90 (1H, d, J=3.1 Hz), 7.59–7.41 (2H, m), 7.14 (1H, d, J=8.6 Hz), 6.99 (1H, dd, J=8.9, 3.5 Hz), 3.72 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238714B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-a82fe8ed802d46da97da38b58e32a54e |
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| Source note | uspto-grants-2007_07 |
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