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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213970Generated: November 2, 2026

Phenylacetylene → HCID 11298050, compound

https://huagongshe.com/reaction/2213970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant1-HexyneHCID 12732—
Reactant2-FuronitrileHCID 69245—
SolventBenzonitrileHCID 7505—
ProductHCID 11298050HCID 1129805069%

Reaction Steps

The procedure was identical to Example 1, with the exception that 1-hexyne (0.450 ml; 0.329 g; 4.00 mmol) was used as a substrate instead of phenylacetylene and 2-furonitrile (0.175 ml; 0.186 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 4 h at 65° C. showed the presence of 1.38 mmol (69% yield) of 2-(1-hexynyl)furan and no remaining 2-furonitrile in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105707B2
Source datasetuspto-grants-2006_09
ORD IDord-a2f8a0b8af5f4f7a82db255b25d6d2d2
Source noteuspto-grants-2006_09