HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-(4-bromo-1h-pyrazol-1-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-(1H-pyrazol-1-yl)pyridine | HCID 5324086 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-(4-bromo-1h-pyrazol-1-yl)pyridine | HCID 11345106 | — |
Reaction Steps
Bromine (10.8 mL, 210 mmol) in AcOH (50 mL) was added carefully to a solution of 2-(1H-pyrazol-1-yl)pyridine (11 g, 70 mmol) in AcOH (100 mL) to give a brown precipitate. After stirring at ambient temperature for 3 h, the resulting reaction mixture was poured into ice and saturated aqueous Na2SO2O5 was added until the liquid phase became clear. The precipitate was removed by filtration and recrystallized from EtOH:H2O to give 2-(4-bromo-1H-pyrazol-1-yl)pyridine as beige crystals. 1H NMR (CD3Cl, 300 MHz) δ 8.61 (1H, s), 8.42 (1H, br. s), 7.94-7.96 (1H, m), 7.84 (1H, ddd), 7.69 (1H, s), 7.21-7.28 (1H, m). MS (ESI) 225 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07569592B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-987b965aa21d4d8bb091e5feb0dd9d06 |
| Source note | uspto-grants-2009_08 |