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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297866Generated: November 1, 2026

2-(Hydroxymethyl)-4-iodophenol → 5-Iodosalicylaldehyde

https://huagongshe.com/reaction/2297866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Hydroxymethyl)-4-iodophenolHCID 12545259—
CatalystHCID 178418406HCID 178418406—
SolventAcetoneHCID 180—
Product5-IodosalicylaldehydeHCID 25261258%

Reaction Steps

To a stirred solution of 2-hydroxy-5-iodobenzyl alcohol (43.5 g, 174.0 mmol) in acetone (700 mL) was added 85% activated manganese(IV) oxide (5 micron, 50 g, 494.0 mmol) and the solution stirred at room temperature for 16 hours. The manganese oxide was removed by filtration through diatomaceous earth and the filtrate concentrated in vacuo. The product was purified by flash silica chromatography (0-20% ethyl acetate in hexanes) The 2-hydroxy-5-iodobenzaldehyde was obtained as a greenish-yellow solid (24.3 g, 58%). A small amount of the 2-hydroxy-5-iodobenzaldehyde was recrystallized from methanol/water to afford an analytical sample and the remainder of the compound was used without further purification: mp 99-101° C. 1H NMR (CDCl3/300 MHz) 9.83 (s, 1H), 7.79 (d, 1H, J=2.2 Hz), 7.77 (dd, 1H, J=8.7 Hz, J=2.2 Hz), 6.81 (d, 1H, J=8.7 Hz). ESHRMS 246.9229 (M−H Calc'd 246.9256).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492390B2
Source datasetuspto-grants-2002_12
ORD IDord-732f940dda17426581618de370394132
Source noteuspto-grants-2002_12