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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213958Generated: October 26, 2026

Benzonitrile → 2-(Phenylethynyl)furan

https://huagongshe.com/reaction/2213958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
Reactant2-FuronitrileHCID 69245—
Product2-(Phenylethynyl)furanHCID 1101925274%

Reaction Steps

The procedure was identical to Example 1, with the exception that 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 18 h at 65° C. showed the presence of 1.26 mmol (74% yield) of 2-(phenylethynyl)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-a4b01b0c6e964a4cacdaf67e42468670
Source noteuspto-grants-2006_09