HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 2-amino-5-bromobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-5-bromobenzoic acid | HCID 79858 | — |
| Reactant | Methyl sulfate(1-) | HCID 4694097 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-amino-5-bromobenzoate | HCID 736224 | 56.7% |
Reaction Steps
MeSO4 (26.3 mL, 0.280 mol) was added to a solution of 2-amino-5-bromobenzoic acid (50.0 g, 0.230 mol) in DMF and Et3N (40 mL, 0.28 mol). The reaction mixture was stirred at rt for 48 h. The mixture was quenched with water, extracted with EtOAc and dried over MgSO4. The solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel (5% EtOAc in petroleum ether) to afford methyl 2-amino-5-bromobenzoate (30 g, 56% yield). 1H NMR (300 MHz, DMSO) δ 7.74 (d, J=2.7, 1H), 7.35 (dd, J=9.0, 2.1, 1H), 6.78-6.73 (m, 3H), 3.77 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039491B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-8fcfff50b2ec4e9a8bf8b8cbe6227b48 |
| Source note | uspto-grants-2011_10 |