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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891443Generated: November 2, 2026

Oxygen → 3-Cyano-4-fluorobenzoic acid

https://huagongshe.com/reaction/1891443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantSodium SulfiteHCID 24437—
ReactantMonobasic potassium phosphateHCID 516951—
Reactant2-Fluoro-5-formylbenzonitrileHCID 2769582—
ReactantSodium ChloriteHCID 23668197—
SolventHydrogen PeroxideHCID 784—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-Cyano-4-fluorobenzoic acidHCID 2773932166.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-cyano-4-fluorobenzaldehyde (45 g, 301 mmol) in CH3CN (450 mL) was added potassium phosphate monobasic (24 g, 176 mmol) in water (225 mL) and 30% hydrogen peroxide in water (30 mL). The reaction mixture was cooled to 0° C. and sodium chlorite (60 g, 663 mmol) in water (450 mL) was added dropwise over 2 h. The resulting yellow suspension was stirred at room temperature until production of oxygen ceased (4 h). Sodium sulfite (30 g, 238 mmol) in water (100 mL) was added and the reaction mixture stirred for 1 h. The reaction was quenched with 2N HCl (500 mL) and the resulting solid was filtered and washed with water. The aqueous phase was extracted with EA (2×500 mL). The combined organic layers were washed with brine (200 mL), dried over MgSO4, concentrated, and combined with the collected solid to produce a total of 48.5 g (97%) of crude 3-cyano-4-fluorobenzoic acid as a white solid. LCMS-ESI (m/z) calculated for C8H4FNO2: 165.0; found 166.1 [M+H]+, tR=2.54 min. 1H NMR (400 MHz, DMSO) δ 13.60 (s, 1H), 8.41 (dd, J=6.3, 2.1 Hz, 1H), 8.30 (ddd, J=8.8, 5.3, 2.2 Hz, 1H), 7.66 (t, J=9.0 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507538B2
Source datasetuspto-grants-2013_08
ORD IDord-5d1ed51bbbda4612a692875fb59fb8b0
Source noteuspto-grants-2013_08