HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-5-nitroanisole → 2-(2-Methoxy-4-nitrophenyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-5-nitroanisole | HCID 101293 | — |
| Reactant | HCID 178418723 | HCID 178418723 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Methoxy-4-nitrophenyl)pyridine | HCID 21956526 | — |
Reaction Steps
A solution of 2-bromo-5-nitroanisole (5.8 g, 25 mmol) in THF (50 mL) was treated with 2-pyridyl-zinc bromide (50 mL of a 0.5M solution in THF, 25 mmol) and Pd(PPh3)4 (1.44 g, 1.25 mmol). The reaction mixture was degassed by bubbling argon through the solution for min and was subsequently heated to reflux for 12 h while under an atmosphere of argon. The cooled reaction mixture was concentrated and purified by flash column chromatography on silica gel eluting with EtOAc:hexanes (1:19 to 2:3) to afford the desired 2-(2-methoxy-4-nitrophenyl)pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105533B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-90633e76986b47c095dae0ecbc32a69a |
| Source note | uspto-grants-2006_09 |