HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-Bromo-n-(2-nitrophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Nitroaniline | HCID 6946 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-n-(2-nitrophenyl)acetamide | HCID 220787 | 92% |
Reaction Steps
2-Bromoacetyl bromide (173 μL, 1.99 mmol) was added dropwise to a solution of 2-nitroaniline (250 mg, 1.81 mmol) and pyridine (293 μL) in CH2Cl2 (9 mL). The reaction mixture was stirred at room temperature for 45 min. The mixture was then diluted with CH2Cl2 (10 mL), washed with aqueous 1 N HCl solution (10 mL), water (10 ml) and brine (10 mL). The organic layer was dried (Na2SO4), filtered and concentrated under reduced pressure to yield the title compound (431 mg, 92% yield) as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07642277B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-21ef7a1460af4c3ba61e2e003c790649 |
| Source note | uspto-grants-2010_01 |