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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 722289Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/722289

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Hydroxymethyl)-4-iodophenolHCID 12545259—
KatalysatorHCID 178418406HCID 178418406—
LösungsmittelAcetoneHCID 180—
Produkt5-IodosalicylaldehydeHCID 25261258%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07138411B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-bba639585cdc46459e309ca40d5ea179
Quellennotizuspto-grants-2006_11