HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 4-(Biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | (1,1'-Biphenyl)-2-ol | HCID 7017 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2-Benzenedicarbonitrile, 3,4,5,6-tetrachloro- | HCID 16057 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(Biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242990B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-dc90e00db95245328fecfee6e85e59a8 |
| Source note | uspto-grants-2016_01 |