HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2-Bromo-thiophen-3-yl)-4-chloro-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | 4-Chloro-2-thiophen-3-yl-Pyridine | HCID 67242223 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Bromo-thiophen-3-yl)-4-chloro-pyridine | HCID 67388329 | — |
Reaction Steps
A solution of 4-chloro-2-thiophen-3-yl-pyridine (755 mg, 3.9 mmol), prepared from 2-thiopheneboronic acid via the method outlined in Example 26, Step A, and N-bromosuccinimide (712 mg, 4 mmol) in DMF (6 mL) was stirred at room temperature for 8 h. The reaction mixture was poured into water and extracted with EtOAc. The organic layer was dried and concentrated to yield a residue. The residue was recrystallized from EtOH to yield 2-(2-bromo-thiophen-3-yl)-4-chloro-pyridine as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022209B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-2799da07b16b442d93b9491ff104195c |
| Source note | uspto-grants-2011_09 |