HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1,1'-Biphenyl)-4-carbonitrile → 2,4-Bisbiphenyl-4-yl-6-(4-bromophenyl)-1,3,5-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1,1'-Biphenyl)-4-carbonitrile | HCID 18021 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 2,4-Bisbiphenyl-4-yl-6-(4-bromophenyl)-1,3,5-triazine | HCID 67335276 | — |
Reaction Steps
1.21 g (0.0091 mol) of aluminium chloride, 1.997 g (0.0091 mol) of 4-bromobenzoyl chloride and 3.42 g (0.01911 mol) of 4-cyanobiphenyl are initially introduced. The solids are dissolved in 80 ml of 1,2-dichlorobenzene. 0.2 ml (0.00274 mol) of thionyl chloride is added. The reaction is carried out at 120° C. for 24 h. After a reaction time of 1 h, 0.9736 g (0.00182 mol) of ammonium chloride is added. As work-up, the mixture is poured into 50 ml of methanol. The white solid is filtered off with suction and recrystallised in chloroform/ethanol. 1.7 g (34%) of clean substance are isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08786181B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-b14db8d517f945cdb0d42715f15623d6 |
| Source note | uspto-grants-2014_07 |