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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594925Generated: October 26, 2026

Acetonitrile → 4-(Biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrile

https://huagongshe.com/reaction/594925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant(1,1'-Biphenyl)-2-olHCID 7017—
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Benzenedicarbonitrile, 3,4,5,6-tetrachloro-HCID 16057—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product4-(Biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrileHCID 117902707—

Reaction Steps

3,4,5,6-tetrachlorophthalonitrile (5 g), 2-phenylphenol (3.201 g), K2CO3 (3.898 g) and acetonitrile (50 ml) are put in a 100 ml flask and then heated and refluxed. When the reaction is complete, the resultant is filtered with tetrahydrofuran (THF) to obtain a solid, the solid is added to a small amount of dichloromethane and dissolved therein, and hexane is added thereto, obtaining a crystallized solid (4-(biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrile). Herein, the obtained solid is washed several times, filtered and vacuum-dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242990B2
Source datasetuspto-grants-2016_01
ORD IDord-dc90e00db95245328fecfee6e85e59a8
Source noteuspto-grants-2016_01