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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714713Generated: October 29, 2026

Tetraethylene Glycol → 3,6,9,12-Tetraoxapentadec-14-en-1-ol

https://huagongshe.com/reaction/1714713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethylene GlycolHCID 8200—
ReactantAllyl iodideHCID 11166—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product3,6,9,12-Tetraoxapentadec-14-en-1-olHCID 1012521452.8%

Reaction Steps

To an anhydrous solution of potassium tert-butoxide (2.3 g, 19.5 mmol) in THF (500 mL), tetraethylene glycol (7.18 g, 37.0 mmol) is added at room temperature. The resulting mixture is stirred for 30 min, and a solution of allyl iodide (3.31 g, 19.7 mmol) in dry THF (60 mL) is added dropwise over 1 h. The reaction mixture is stirred for 30 h and filtered through a silica plug (10 g) using ethyl acetate (800 mL) to elute all product. After evaporation of the solvent in vacuo, the product is purified by column chromatography using a solvent gradient petrol ether/ethyl acetate 10:1 to ethyl acetate 100% yielding a colourless oil (2.41 g, 10.3 mmol, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799524B2
Source datasetuspto-grants-2010_09
ORD IDord-5947f45e52264e4e80a20a2d47b7a8ac
Source noteuspto-grants-2010_09