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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213967Generated: November 2, 2026

Phenylacetylene → HCID 11470391, compound

https://huagongshe.com/reaction/2213967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant2-NaphthalenecarbonitrileHCID 11944—
Reactant1-OctyneHCID 12370—
SolventBenzonitrileHCID 7505—
ProductHCID 11470391HCID 1147039199%

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 2-naphthonitrile (0.306 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 22 h at 65° C. showed the presence of 1.98 mmol (99% yield) of 2-(1-octynyl)naphthalene and no remaining 2-naphthonitrile in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105707B2
Source datasetuspto-grants-2006_09
ORD IDord-44b32b9f9a7c46e9ac8df5380d079e06
Source noteuspto-grants-2006_09