HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2-Chloro-thiophen-3-yl)-4-chloro-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | 4-Chloro-2-thiophen-3-yl-Pyridine | HCID 67242223 | — |
| Product | 2-(2-Chloro-thiophen-3-yl)-4-chloro-pyridine | HCID 67388275 | — |
Reaction Steps
To a solution of 4-chloro-2-thiophen-3-yl-pyridine (410 mg, 2.1 mmol), prepared as described in Example 26, Step A, using 2-thiopheneboronic acid, in CH2Cl2 (10 mL), was added SO2Cl2 (1 M in CH2Cl2, 3 mL). The resulting mixture was stirred at room temperature for 8 h, then was poured into water and extracted with CH2Cl2. The organic layer was dried and concentrated to yield a residue. The residue was purified by preparative TLC (hexanes/EtOAc) to yield 2-(2-chloro-thiophen-3-yl)-4-chloro-pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022209B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-a81592eec31b4b928beb0a15b97ee6f8 |
| Source note | uspto-grants-2011_09 |