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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334777Generated: October 29, 2026

2-Bromopyridine → 2-(5-Chloropent-1-ynyl)pyridine

https://huagongshe.com/reaction/334777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant1-Pentyne, 5-chloro-HCID 84308—
Product2-(5-Chloropent-1-ynyl)pyridineHCID 6659855761%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 190(F), from 2-bromopyridine (948 mg, 6.0 mmol) and 5-chloropent-1-yne (620 mg, 6.0 mmol). The crude residue was purified over silicagel chromatography (prepacked 25 g silicagel column, Cyclohexane/AcOEt: from 100/0 to 80/20 as eluent) to afford 655 mg of 2-(5-chloropent-1-ynyl)pyridine as a yellow oil (Yield: 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-be5754d4b9bd49b2a9477925011c81d3
Source noteuspto-grants-2014_11