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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910674Generated: October 26, 2026

Water → 2-(2-Chloro-thiophen-3-yl)-4-chloro-pyridine

https://huagongshe.com/reaction/910674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactant4-Chloro-2-thiophen-3-yl-PyridineHCID 67242223—
Product2-(2-Chloro-thiophen-3-yl)-4-chloro-pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022209B2
Source datasetuspto-grants-2011_09
ORD IDord-a81592eec31b4b928beb0a15b97ee6f8
Source noteuspto-grants-2011_09