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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033137Generated: October 25, 2026

Water → 1-(3-Iodophenoxy)-6-(2,4,6-triiodophenoxy)-hexane

https://huagongshe.com/reaction/1033137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3-IodophenolHCID 12272—
Reactant6-(2,4,6-Triiodophenoxy)-1-chlorohexaneHCID 15224801—
SolventDimethylformamideHCID 6228—
Product1-(3-Iodophenoxy)-6-(2,4,6-triiodophenoxy)-hexaneHCID 1522480254%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of potassium carbonate (3.0 g, 21.9 mmol, 1.1 eq), 3-iodophenol (4.4 g, 19.9 mmol) and 6-(2,4,6-triiodophenoxy)-1-chlorohexane (11.75 g, 19.9 mmol) in 50 ml of DMF was heated to 110° C. for 1.5 hours and then cooled. The mixture was poured into water and extracted with ethyl acetate. The organic layer was dried (magnesium sulfate) and evaporated to give a solid which was filtered through basic alumina (hexanes-ethyl acetate). The filtrate was concentrated under vacuum leaving the crude product as a solid. Recrystallization from cyclohexane afforded 8.29 g (54%) of the desired product after drying at room temperature under high vacuum, mp 65°-66° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310538
Source datasetuspto-grants-1994_05
ORD IDord-b6a7fdf379df4f7fbf91fa556a2b3282
Source noteuspto-grants-1994_05