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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 914642Erstellt: 26. Oktober 2026

2,4,6-Triiodophenol → 12-(2,4,6-Triiodophenoxy)dodecanoic acid

https://huagongshe.com/reaction/914642

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,6-TriiodophenolHCID 11862—
EduktPotassium HydroxideHCID 14797—
Edukt12-Bromododecanoic AcidHCID 175468—
LösungsmittelEthanolHCID 702—
Produkt12-(2,4,6-Triiodophenoxy)dodecanoic acidHCID 1214874760,8%

Reaktionsschritte

Ethanol (70 mL) was added with 12-bromododecanoic acid (4.8 g) and 2,4,6-triiodophenol (9.1 g) and the mixture was refluxed for dissolution. The solution was added with potassium hydroxide (2.2 g) and stirred for 12 hours. The precipitates obtained were separated by filtration, washed with ethanol and added with chloroform and 1 N hydrochloric acid to conduct extraction with chloroform twice. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was removed, and the resulting residue was purified by silica gel column chromatography to obtain 12-(2,4,6-triiodophenoxy)dodecanoic acid (7.0 g, yield: 60%). In the same manner as the synthetic method of 12-(2,4,6-triiodophenoxy)dodecanoic acid, 16-(2,4,6-triiodophenoxy)hexadecanoic acid was synthesized from 16-bromohexadecanoic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07264790B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-dfd31c93e20e4077a2c961a6ff6f8a14
Quellennotizuspto-grants-2007_09