Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213969Generated: November 1, 2026

Phenylacetylene → HCID 11217767, compound

https://huagongshe.com/reaction/2213969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant4-ChlorobenzonitrileHCID 12163—
Reactant1-HexyneHCID 12732—
CatalystHCID 11831501HCID 11831501—
SolventBenzonitrileHCID 7505—
ProductHCID 11217767HCID 1121776765%

Reaction Steps

The procedure was identical to Example 2, with the exception that 1-hexyne (0.450 ml; 0.329 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 20 h at 65° C. showed the presence of 1.29 mmol (65% yield) of 1-chloro-4-(1-hexynyl)benzene, 0.10 mmol 1,4-bis(1-hexynyl)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-d9a3b0de11cb4ccf8303f120daa1260a
Source noteuspto-grants-2006_09