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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213965Generated: November 1, 2026

4-Cyanopyridine → HCID 11229223, compound

https://huagongshe.com/reaction/2213965

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanopyridineHCID 7506—
ReactantPhenylacetyleneHCID 10821—
Reactant1-OctyneHCID 12370—
SolventBenzonitrileHCID 7505—
ProductHCID 11229223HCID 1122922380%

Reaction Steps

The procedure was identical to Example 2, with the exception that 1-octyne (0.590 ml; 0.441 g; 4.00 mmol) was used as a substrate instead of phenylacetylene and 4-cyanopyridine (0.208 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 21 h at room temperature showed the presence of 1.60 mmol (80% yield) of 4-(1-octynyl)pyridine and no remaining 4-cyanopyridine in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105707B2
Source datasetuspto-grants-2006_09
ORD IDord-886c6ea6b49948b4bd3f9d6aeea1c775
Source noteuspto-grants-2006_09