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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334530Generated: October 27, 2026

2-Chloroquinoline → 2-(4-Phenylbut-1-ynyl)quinoline

https://huagongshe.com/reaction/334530

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroquinolineHCID 11928—
Reactant4-Phenyl-1-butyneHCID 123360—
Product2-(4-Phenylbut-1-ynyl)quinolineHCID 1159408037%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 1, from 2-chloroquinoline (300 mg, 1.83 mmol) and 1-(but-3-ynyl)benzene (200 mg, 1.54 mmol). The crude residue was purified by flash chromatography (cyclohexane/AcOEt 95:5) to yield 148 mg (0.57 mmol, 37%) of 2-(4-phenylbut-1-ynyl)quinoline as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-b435edc753e945889c143c57f41cb8ac
Source noteuspto-grants-2014_11