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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910675Generated: October 26, 2026

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

https://huagongshe.com/reaction/910675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactant4-Chloro-2-thiophen-3-yl-PyridineHCID 67242223—
SolventDimethylformamideHCID 6228—
Product2-(2-Bromo-thiophen-3-yl)-4-chloro-pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022209B2
Source datasetuspto-grants-2011_09
ORD IDord-2799da07b16b442d93b9491ff104195c
Source noteuspto-grants-2011_09