HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333670Generated: October 25, 2026
Ethanol → 2-(2-(2-(2-Azidoethoxy)ethoxy)ethoxy)ethyl methanesulfonate
https://huagongshe.com/reaction/333670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 1,11-Bis(methanesulfonyloxy)-3,6,9-trioxandecane | HCID 3637875 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-(2-(2-Azidoethoxy)ethoxy)ethoxy)ethyl methanesulfonate | HCID 14827673 | 47.1% |
Reaction Steps
Sodium azide (1.0 g) is added to a solution of tetraethyleneglycol dimethanesulphonate (5.25 g, 15 mmol), obtained according to A. W. Chwabacher et al. (J. Org. Chem. 1998, 65(5), 1717), in 18 mL of 95° ethanol. The reaction mixture is taken to reflux for 24 hours. Then the solvent is evaporated off, the reaction crude is added to 100 mL of salt water and extracted with ether 3×100 mL. The organic phase is dried over MgSO4, filtered and concentrated under reduced pressure. The residue obtained is purified by chromatography on a silica column using a gradient of AcOEt in hexane (1/1 to 3/1) as eluents. 2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl mono-methanesulphonate 47 (2.10 g, 47%) is obtained, which is used directly in the following stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883763B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-332d2bdcab9e4802a75330b5ac5759c4 |
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| Source note | uspto-grants-2014_11 |
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