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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128891Generated: October 25, 2026

Ethyl Acetate → 1-(3-Iodophenoxy)-3,6,9-trioxadecane

https://huagongshe.com/reaction/128891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant3-IodophenolHCID 12272—
Reactant2-(2-(2-Methoxyethoxy)ethoxy)ethyl methanesulfonateHCID 12621272—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Product1-(3-Iodophenoxy)-3,6,9-trioxadecaneHCID 1898700361.6%

Reaction Conditions

Temperature68 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466435
Source datasetuspto-grants-1995_11
ORD IDord-7e492b043bfe4ec695a995ef1030b663
Source noteuspto-grants-1995_11