HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetraethylene Glycol → 3,6,9,12-Tetraoxapentadec-14-en-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetraethylene Glycol | HCID 8200 | — |
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,6,9,12-Tetraoxapentadec-14-en-1-ol | HCID 10125214 | 52.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07799524B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-5947f45e52264e4e80a20a2d47b7a8ac |
| Source note | uspto-grants-2010_09 |