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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810859Generated: November 2, 2026

Tetrafluoroboric acid → 3-Fluoro-5-hydroxy-4-methoxybenzoic acid

https://huagongshe.com/reaction/1810859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroboric acidHCID 28118—
Reactant3-Acetoxy-5-amino-4-methoxy-benzoic acidHCID 12924026—
ReactantSodium NitriteHCID 23668193—
Product3-Fluoro-5-hydroxy-4-methoxybenzoic acidHCID 67076592—

Reaction Steps

The compound of step 1 (2.0 g, 8.88 mmol) was dissolved in aqueous tetrafluoroboric acid (48%, 4.5 ml), sodium nitrite (612 mg, 8.88 mmol) was added at 0° C., and the mixture was stirred at room temperature for 60 min. The volatiles were evaporated, toluene was added to the oily residue and the mixture was heated at 100° C. for 4 h. The mixture was partitioned between EA and 2 N hydrochloric acid, the aqueous phase extracted with EA, and the combined organic extracts were dried over sodium chloride, decanted and evaporated to dryness. The residue was purified by preparative RP HPLC (water/ACN gradient) to give 170 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362073B2
Source datasetuspto-grants-2013_01
ORD IDord-6adcb024f17049c7807298d2f74c2d87
Source noteuspto-grants-2013_01