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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855022Generated: October 30, 2026

Iodine → 2-Hydroxy-3-iodo-4-methoxybenzaldehyde

https://huagongshe.com/reaction/855022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthyl AcetateHCID 8857—
ReactantMetaperiodic acidHCID 65185—
Reactant2-Hydroxy-4-MethoxybenzaldehydeHCID 69600—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Hydroxy-3-iodo-4-methoxybenzaldehydeHCID 1908905749%

Reaction Conditions

Temperature68 °C

Reaction Steps

To a solution of 4.0 g (26.3 mmol) of 2-hydroxyl-4-methoxybenzaldehyde in 30 mL of ethanol was added 1.87 g (7.4 mmol) of iodine, followed by addition of a solution of 6 g (26.3 mmol) of periodic acid in 10 mL of water. The resulting dark yellow solution was heated to 68° C. for two h. After cooling to room temperature, the reaction was added to 300 mL of ethyl acetate. The resulting organic solution was washed with saturated aqueous solution of sodium sulfite, washed with brine and dried over anhydrous magnesium sulfate. After removing the volatiles, the crude products were purified by silica chromatography to afford 1.8 g (49%) of a light yellow solid: 1H NMR(CDCl3/400 MHz,) 12.18(s, 1H), 9.63(s, 1H), 7.53(d, J=8.4 Hz, 1H), 6.56(d, J=8.4 Hz, 1H), 3.99(s, 3H). 13C NMR (CDCl3/400 MHz) 194.2, 165.3, 163.0, 136.3, 116.1, 103.6, 57.2. MS (ESI+) 278.9(M+1, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-bd8a5cc0bcc44aada70c09ced8b4b17c
Source noteuspto-grants-2007_08