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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Iodophenol | HCID 12272 | — |
| Reactant | 6-(2,4,6-Triiodophenoxy)-1-chlorohexane | HCID 15224801 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(3-Iodophenoxy)-6-(2,4,6-triiodophenoxy)-hexane | HCID 15224802 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05310538 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-b6a7fdf379df4f7fbf91fa556a2b3282 |
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| Source note | uspto-grants-1994_05 |
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