HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033136Generated: October 25, 2026
Ethyl Acetate → 1-(3-Iodophenoxy)-3,6,9-trioxadecane
https://huagongshe.com/reaction/1033136
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 | (Methanesulfonyl)-oxyl-3,6,9-trioxadecane | HCID 86747821 | — |
| 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)-oxyl-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), 1 N 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 | US05310538 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-fa7feb9a31d147e0a598dc652d9cfc17 |
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| Source note | uspto-grants-1994_05 |
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