HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 5-Bromo-2,4-dimethoxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2,4-dimethoxypyridine | HCID 817731 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Potassium Bromide | HCID 253877 | — |
| Product | 5-Bromo-2,4-dimethoxypyridine | HCID 18788708 | 70% |
Reaction Steps
According to Scheme 23 Step 2: To a solution of KOH (0.5 eq, 0.8 mmol, 40 mg) in water (75 mL) was added 2,4-dimethoxypyridine (1 eq, 2.00 mmol, 0.21 g) followed by the dropwise addition of Br2 (1 eq, 2.00 mmol, 0.20 g) in 1M aqueous KBr solution (75 mL). The reaction was stirred at room temperature for 5 hours and then poured onto water (10 mL) and extracted with CH2Cl2 (3×10 mL). The combined organic fractions were dried (MgSO4), filtered and concentrated under reduced pressure to afford 5-bromo-2,4-dimethoxypyridine (1.40 mmol, 0.30 g, 70%) as a colorless oil. The crude product was reacted on.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399493B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-b916d5ddb70b4b1f919489a5069259ac |
| Source note | uspto-grants-2013_03 |