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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroboric acidHCID 28118—
ReactantSodium NitriteHCID 23668193—
ReactantMethyl 2-[(5-aminopyridin-2-yl)oxy]-5-chlorobenzoateHCID 69415937—
SolventWaterHCID 962—
ProductMethyl 5-chloro-2-[(5-fluoropyridin-2-yl)oxy]benzoateHCID 6941881142%

Reaction Conditions

Temperature140 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238714B2
Source datasetuspto-grants-2007_07
ORD IDord-a82fe8ed802d46da97da38b58e32a54e
Source noteuspto-grants-2007_07