Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213952Generated: October 31, 2026

Benzonitrile → Diphenylacetylene

https://huagongshe.com/reaction/2213952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
ReactantPhenylacetyleneHCID 10821—
ReactantTridecaneHCID 12388—
ReactantButyllithiumHCID 178418339—
CatalystBenzonitrileHCID 7505—
CatalystZinc bromideHCID 10421208—
Solvent2-MethyltetrahydrofuranHCID 7301—
SolventTetrahydrofuranHCID 8028—
ProductDiphenylacetyleneHCID 1039056%

Reaction Steps

A solution of phenylacetylene (0.439 ml; 0.409 g; 4.00 mmol) in THF (2 ml) was treated at 0° C. with n-butyllithium (1.6 ml; 4.0 mmol; 2.5 M in hexanes) and the resulting solution was allowed to warm to room temperature for 10 min. The solution was cooled to 0° C., then treated with a solution of ZnBr2 (0.901 g; 4.00 mmol) in THF (2 ml) and allowed to warm to room temperature for 30 min. Solvent was removed in vacuo, then 2-methyltetrahydrofuran (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 2-methyltetrahydrofuran (2 ml). The reaction mixture was then heated to 65° C. and stirred for 5 days; then a sample was withdrawn and quenched in a mixture of 1 M sodium citrate (aq) and MTBE.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 1.12 mmol (56% yield) of diphenylacetylene and 0.10 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-115968d6f02747aca6ce632d48153673
Source noteuspto-grants-2006_09