HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 2-(Nitrooxy)ethan-1-aminium nitrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Nitrooxy)ethan-1-aminium nitrate | HCID 21075946 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
2-Hydroxyethylamine (5 g, 81.9 mmol) in EtOAc (40 mL) was added drop-wise to a mixture of fuming HNO3 (18 g, 12 mL, 0.29 mol) and Ac2O (54 g, 50 mL, 0.53 mol) at −10° C. The reaction mixture was stirred at 0° C. for 10 minutes and at room temperature for 10 minutes. The solvent was evaporated in high vacuo at 40° C. The residue was sonicated with ether. The solid was filtered and washed with hexane to give the title compound as a white solid. Mp 92-94° C. 1H NMR (300 MHz, d6-DMSO) δ 7.71-8.25 (bs, 3H), 4.72 (t, J=5.0 Hz, 2H), 3.23 (d, J=5.0 Hz, 2H). 13C NMR (75 MHz, d6-DMSO) δ 70.9, 37.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088762B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-b4e169c47ad64c5594dc7637c431dec8 |
| Source note | uspto-grants-2012_01 |