HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 69010851, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Amino-4,5-dimethoxybenzonitrile | HCID 735967 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69010851 | HCID 69010851 | 23% |
Reaction Steps
Under N2 suspend 2-amino-4,5-dimethoxybenzonitrile (2.0 g, 12.25 mmol) in ethanol (50 mL), and add sodium bicarbonate (3.09 g, 36.78 mmol) in one portion. By syringe, slowly add ethyl bromoacetate (2.72 mL, 24.5 mmol), and then sodium iodide (10 mg). Heat the reaction at 65° C. and then cool to ambient temperature. Filter the resulting solid and wash with ethyl acetate to dissolve the organics. Concentrate the filtrate to obtain 0.66 g (23%) of the title compound; MS 265(M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07169925B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-3c0cf2c52d1440b38ef3bb0a15b71d85 |
| Source note | uspto-grants-2007_01 |