HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53493Generated: October 25, 2026
Water → (E)-1-(2,4,6-triiodophenoxy)-3,7-dimethyl-2,6-octadiene
https://huagongshe.com/reaction/53493
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,6-Triiodophenol | HCID 11862 | — |
| Reactant | 2,6-Octadiene, 1-bromo-3,7-dimethyl-, (2E)- | HCID 5365867 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-1-(2,4,6-triiodophenoxy)-3,7-dimethyl-2,6-octadiene | HCID 15343331 | 87% |
Reaction Steps
A mixture of triiodophenol (10.0 g, 21.2 mmol), milled potassium carbonate (3.1 g, 22.5 mmol, 1.06 eq) and geranyl bromide (4.0 ml, 20.2 mmol) in dimethyl formamide (25 ml) was heated to 50° C. for 2 hrs and cooled. The mixture was poured into 300 ml of water and extracted with ethyl acetate. The ethyl acetate extract was filtered through a short pad of silica gel, then alumina, eluting with ethyl acetate-hexanes (1:1). The eluent was concentrated under high vacuum to give the product in 87% yield as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05620677 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-e22a45abcb974474bdf8c81aa359d759 |
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| Source note | uspto-grants-1997_04 |
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