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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213954Generated: November 3, 2026

Benzonitrile → Diphenylacetylene

https://huagongshe.com/reaction/2213954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
ReactantPhenylacetyleneHCID 10821—
ReactantTridecaneHCID 12388—
ReactantButyllithiumHCID 178418339—
CatalystZinc bromideHCID 10421208—
SolventTetrahydrofuranHCID 8028—
ProductDiphenylacetyleneHCID 1039065%

Reaction Steps

A solution of phenylacetylene (0.659 ml; 0.613 g; 6.00 mmol) in THF (2 ml) was treated at 0° C. with n-butyllithium (2.4 ml; 6.0 mmol; 2.5 M in hexanes) and the resulting solution was allowed to warm to room temperature for 15 min. The solution was cooled to 0° C., then treated with a solution of ZnBr2 (1.35 g; 6.00 mmol) in THF (3 ml) and allowed to warm to room temperature for 30 min. Solvent was removed in vacuo, then THF (2 ml) was added. This solution was then added to a room temperature solution of benzonitrile (0.204 ml; 0.206 g; 2.00 mmol), dichlorobis(trimethylphosphine)nickel (0.0564 g; 10 mol %), and tridecane (0.244 ml; 0.184 g; 1.00 mmol) in THF (1 ml). The reaction mixture was then heated to 65° C. and stirred for 65 h; then a sample was withdrawn and quenched in a mixture of 1 M sodium citrate (aq) and MTBE. GC analysis of the organic phase of the hydrolyzed reaction sample showed the presence of 1.30 mmol (65% yield) of diphenylacetylene and 0.20 mmol of benzonitrile remaining in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105707B2
Source datasetuspto-grants-2006_09
ORD IDord-ede95e39d0a4412c8a7a753ef262111e
Source noteuspto-grants-2006_09