HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396410Generated: October 25, 2026
Ethyl Acetate → 1-(3-Iodophenoxy)-3,6,9-trioxadecane
https://huagongshe.com/reaction/2396410
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Iodophenol | HCID 12272 | — |
| Reactant | 2-(2-(2-Methoxyethoxy)ethoxy)ethyl methanesulfonate | HCID 12621272 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-(3-Iodophenoxy)-3,6,9-trioxadecane | HCID 18987003 | 61.6% |
Reaction Steps
To a solution of 1-[(methanesulfonyl)-oxy]-3,6,9-trioxadecane (11.6 g, 47.9 mmol) in dry DMF (145 ml) was added 3-iodophenol (10.6 g, 48.2 mmol) and potassium carbonate (6.6 g, 47.8 mmol). The reaction was immersed in an oil bath which was warmed to 68° C. over a period of 0.5 hr. The reaction was stirred at this temperature under an N2 atmosphere for 16 hrs and then at 82° C. for an additional 2 hrs. At the end of this period, the reaction was cooled, diluted with DMF, filtered through a pad of celite and evaporated in vacuo. The resulting residue was taken up into ethyl acetate (500 ml), washed with water (200 ml), 1N aqueous sodium hydroxide (200 ml) and brine (200 ml), dried (Na2SO4), filtered and evaporated in vacuo to provide a light brown oil. Flash column chromatography (silica, 1:3 to 1:2; EtOAc:hexane) provided 1 -(3-iodophenoxy)-3,6,9-trioxadecane as a light yellow oil (10.8 g, 37.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05492687 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-768ad146edfe4a3d80b37eefadb6d2a1 |
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| Source note | uspto-grants-1996_02 |
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