HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → [1,1'-Biphenyl]-2-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | o-Phenylbenzoic acid | HCID 70357 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | [1,1'-Biphenyl]-2-carbonyl chloride | HCID 12563768 | — |
Reaction Steps
Under a dry nitrogen atmosphere 10 g (0.05 mole) of 2-biphenylcarboxylic acid was dissolved with stirring in 116 ml of dry toluene. Pyridine, 4.2 g (0.054 mole), was then added to the reaction mixture followed by 6.4 g (0.054 mole) of thionyl chloride. The reaction mixture was stirred at room temperature for two hours, then filtered to remove a white precipitate. The toluene was removed from the filtrate under reduced pressure to give [1,1'-biphenyl]-2-carbonyl chloride as a liquid residue, which was used without purification in Step B below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04473709 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-0cb3e080d794456cb7fa51d3ea589eb7 |
| Source note | uspto-grants-1984_09 |