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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293259Generated: October 26, 2026

Hydrochloric Acid → 5-Chloro-2-[(5-fluoropyridin-3-yl)oxy]benzoic acid

https://huagongshe.com/reaction/1293259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 5-chloro-2-[(5-fluoropyridin-3-yl)oxy]benzoateHCID 69418031—
SolventMethanolHCID 887—
Product5-Chloro-2-[(5-fluoropyridin-3-yl)oxy]benzoic acidHCID 6941584981.4%

Reaction Steps

To a solution of methyl 5-chloro-2-[(5-fluoropyridin-3-yl)oxy]benzoate (80 mg, 0.28 mmol) in methanol (2 mL) was added 2 M sodium hydroxide aqueous solution (2 mL) and the reaction mixture was stirred at room temperature for 12 h. The reaction mixture was acidified with 2 M hydrochloric acid (2.5 mL). The precipitate was collected by filtration to afford 61 mg (80%) of the title compound: 1H-NMR (CDCl3) δ 8.24 (1H, br.s), 8.19 (1H, br.s), 8.07 (1H, d, J=2.6 Hz), 7.56 (1H, d, J=8.8, 2.6 Hz), 7.06 (1H, d, J=8.8 Hz), 6.98 (1H, td, J=9.4, 2.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238714B2
Source datasetuspto-grants-2007_07
ORD IDord-0410c99ae4774f83acc20ad423797207
Source noteuspto-grants-2007_07