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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213962Generated: November 2, 2026

Phenylacetylene → 1-chloro-4-(1-octynyl)benzene

https://huagongshe.com/reaction/2213962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant4-ChlorobenzonitrileHCID 12163—
Reactant1-OctyneHCID 12370—
CatalystHCID 11748437HCID 11748437—
SolventBenzonitrileHCID 7505—
Product1-chloro-4-(1-octynyl)benzeneHCID 1084660470.5%

Reaction Steps

The procedure was identical to Example 1, 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-chlorobenzonitrile (0.275 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 23 h at 65° C. showed the presence of 1.41 mmol (70% yield) of 1-chloro-4-(1-octynyl)benzene, 0.11 mmol 1,4-bis(1-octynyl)benzene and no remaining 4-chlorobenzonitrile in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105707B2
Source datasetuspto-grants-2006_09
ORD IDord-312db37ac42b4b2ab5e379071f40b6f9
Source noteuspto-grants-2006_09