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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214845Generated: October 30, 2026

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

https://huagongshe.com/reaction/2214845

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 numberUS07109211B2
Source datasetuspto-grants-2006_09
ORD IDord-7848df34e0374bfa86b87f4d51778ee7
Source noteuspto-grants-2006_09