HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Methyl 2-amino-2-(furan-2-yl)acetate hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Methyl 2-(((benzyloxy)carbonyl)amino)-2-(furan-2-YL)acetate | HCID 14085234 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 2-amino-2-(furan-2-yl)acetate hydrobromide | HCID 118647338 | 99.1% |
Reaction Steps
To magnetically stirred 33 wt % hydrogen bromide (2.00 ml, 11.04 mmol) in acetic acid was added methyl 2-(((benzyloxy)carbonyl)amino)-2-(furan-2-yl)acetate (579 mg, 2 mmol). After stirring at room temperature for 1 hr, 25 mL of anhydrous ether was added to give methyl 2-amino-2-(furan-2-yl)acetate hydrobromide (468 mg, 1.983 mmol, 99% yield) as a grey solid. 1H NMR (400 MHz, DMSO-d6) δ 8.93 (s, 2H), 7.81 (dd, J=1.8, 0.8 Hz, 1H), 6.69 (m, 1H), 6.57 (dd, J=3.3, 1.9 Hz, 1H), 5.61 (s, 1H), 3.78 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353060B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-dd52a65ef8ba42229851d9563121ab8a |
| Source note | uspto-grants-2016_05 |