HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Benzyl 2-bromo-5-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-nitrobenzoic acid | HCID 243025 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Benzyl Bromide | HCID 7498 | — |
| Product | Benzyl 2-bromo-5-nitrobenzoate | HCID 19038758 | 187.7% |
Reaction Steps
Under an atmosphere of argon, to a solution of 2-bromo-5-nitrobenzoic acid (5.14 g) in DMF, benzyl bromide (2.73 mL) and potassium carbonate (4.33 g) were added. The mixture was stirred for 30 minutes at room temperature. To the reaction mixture, water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and concentrated. The residue was washed with hexane/ethyl acetate to give the title compound (6.59 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576129B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-096c688eeb30442b9eadb70c82d7af4a |
| Source note | uspto-grants-2009_08 |