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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213971Generated: October 25, 2026

Phenylacetylene → 2-(3,3-Dimethyl-1-butynyl)furan

https://huagongshe.com/reaction/2213971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant3,3-Dimethyl-1-butyneHCID 13512—
Reactant2-FuronitrileHCID 69245—
SolventBenzonitrileHCID 7505—
Product2-(3,3-Dimethyl-1-butynyl)furanHCID 1146915391%

Reaction Steps

The procedure was identical to Example 1, with the exception that 3,3-dimethyl-1-butyne (0.488 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 16 h at 65° C. showed the presence of 1.82 mmol (91% yield) of 2-(3,3-dimethyl-1-butynyl)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-bf8524f53d9c47cea6c4c074f8715e15
Source noteuspto-grants-2006_09