HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-2-chloro-3-nitropyridine → 5-Bromo-2-methoxy-3-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-2-chloro-3-nitropyridine | HCID 7019412 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Bromo-2-methoxy-3-nitropyridine | HCID 15645664 | — |
Reaction Steps
A solution of 20.0 g (84.2 mmol) 5-bromo-2-chloro-3-nitro-pyridine in 50 mL MeOH is cooled to 0° C. and 15.8 mL (84.2 mmol) of a NaOMe solution in MeOH (30%) is added drop wise. The mixture is stirred at RT over night and then stirred under reflux for 24 h. The precipitate is filtered off, suspended in water and the suspension is stirred for 1 h. The product is filtered off and dried und vacuum at 60° C. Yield: 18.7 g (95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598157B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-4f822d449d3f4c0da294cfa7942de7b4 |
| Source note | uspto-grants-2013_12 |