HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Chloroethoxy)ethanol → 2-(2-Azidoethoxy)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Chloroethoxy)ethanol | HCID 12361 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Azidoethoxy)ethan-1-ol | HCID 11400789 | 95.3% |
Reaction Steps
A solution of 2-(2-chloro-ethoxy)-ethanol (15 g, 0.12 mol) and sodium azide (15.7 g, 2 equiv.) in H2O (50 ml) was heated at 90° C. for 16 h. The reaction mixture was cooled down to RT then extracted with CH2Cl2 (6×50 ml). The combined organic layers were dried over MgSO4 and filtrated. The solvents were removed under reduced pressure to give azide 2 as a colorless liquid (15 g, 95%). 1H and 13C NMR spectra matched the literature data (Cheng, H. et al. J. Med. Chem. 2005, 48, 645-653).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073969B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-bb483a33c7a24b8ea90126da72e4e756 |
| Source note | uspto-grants-2015_07 |