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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459257Generated: October 30, 2026

Potassium Iodide → 2-Fluoro-4-hydroxybenzaldehyde

https://huagongshe.com/reaction/459257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-Fluoro-4-methoxybenzaldehydeHCID 2734873—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-Fluoro-4-hydroxybenzaldehydeHCID 58724629%

Reaction Conditions

Temperature40 °C

Reaction Steps

2-Fluoro-4-methoxy-benzaldehyde (1 g, 6.49 mmol) was added to a suspension of anhydrous potassium iodide (2.15 g, 13 mmol) and aluminum trichloride (1.04 g, 7.8 mmol) in anhydrous toluene (10 mL), and the mixture was stirred at 40° C. for 3 hours. Aluminum trichloride (2.15 g, 13 mmol) and anhydrous potassium iodide (0.86 g, 6.49 mmol) were added, and the mixture was stirred for 3 hours. The mixture was diluted with water (10 mL) and extracted with ethyl acetate (5×20 mL). The combined organic layers were dried (MgSO4), filtered, and concentrated under vacuum. The residue was purified by silica gel chromatography (silica gel, hexanes/ethyl acetate 4:1) to give 2-fluoro-4-hydroxy-benzaldehyde as a white solid (260 mg, 29%). 1H NMR (200 MHz, Acetone-d6): δ 10.08 (s, 1H), 9.77 (b, 1H), 7.69 (t, 1H, J=8.4), 6.78 (dd, 1H, J=8.8, 2.6), 6.65 (dd, 1H, J=12.5, 2.2)ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192982B2
Source datasetuspto-grants-2007_03
ORD IDord-b0f443139d904a31b57a0d63f772bb70
Source noteuspto-grants-2007_03