HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 3-(Benzyloxy)-5-chloro-2-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-Chloro-2-nitropyridin-3-ol | HCID 18765698 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Benzyloxy)-5-chloro-2-nitropyridine | HCID 67369437 | 91% |
Reaction Steps
1-(Bromomethyl)benzene (7.905 ml, 66.46 mmol) was added to a mixture of cesium carbonate (21.65 g, 66.46 mmol) and 5-chloro-2-nitropyridin-3-ol (11.6 g, 66.46 mmol) in DMF (50 mL). The reaction mixture was stirred overnight at ambient temperature, then partitioned between ethyl acetate and water, washed with water and brine, dried, and concentrated to afford 3-(benzyloxy)-5-chloro-2-nitropyridine (16.0 g, 91.0% yield) as a light yellow powder. 1H NMR (CDCl3) δ 5.25 (s, 2H), 7.41 (m, 5H), 7.53 (s, 1H), 8.04 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933077B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-7fa26f5191db426f9ea470beb4b8f849 |
| Source note | uspto-grants-2015_01 |