HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → [3-(Azidomethyl)oxetan-3-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | [3-(Bromomethyl)oxetan-3-yl]methanol | HCID 529264 | — |
| Solvent | Water | HCID 962 | — |
| Product | [3-(Azidomethyl)oxetan-3-yl]methanol | HCID 22404019 | 94% |
Reaction Steps
A mixture of sodium azide (9.5 g, 0.14 mol), 3-bromomethyl-3-hydroxymethyloxetane (24.0 g, 0.14 mol), 20 mL of acetone and 20 mL of water was refluxed for 12 h. The acetone was evaporated and the resulting residue was extracted with two portion of 40 mL of ethyl acetate. The combined organic extracts were dried over magnesium sulfate (MgSO4). The solvent was removed by evaporation. 18.0 g, representing a 94% yield, of 3-azidomethyl-3-hydroxymethyloxetane were obtained as an oil. This oil was found to be essentially pure by gas-liquid chromatography (GLC) analysis. NMR: 1H NMR 3.70 (s, 2H), 3.84 (d, J=4.9 Hz, 2H), 4.44 (s, 4H); NMR 44.283, 53,852, 64,073, 76.227.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05489700 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-30c9d85839fb4bb18795e1d280c3439d |
| Source note | uspto-grants-1996_02 |