HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 2,3,4,6-Tetrafluorobiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 2,3,4,6-Tetrafluoroaniline | HCID 123048 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 2,3,4,6-Tetrafluorobiphenyl | HCID 12853049 | — |
Reaction Steps
A stirred solution of 2,3,4,6-tetrafluoroaniline (50 g, 0.30 mole) in benzene (236.6 g, 3.03 mole) was heated under reflux. During a 45 minute period, t-butyl nitrite (46.8 g, 0.455 mole) was added to the reaction mixture. After complete addition the mixture was heated at reflux for 23/4 hours. n-Heptane (1 l) was added, and the solvent was distilled from the reaction flask until a head temperature of 101° was reached. The pot residue was cooled and subjected to column chromatography on silica gel, elution first with n-heptane, then toluene, to give 2,3,4,6-tetrafluoro-[1,1'-biphenyl] (mp, 89°-90°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04402973 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-baf51e718bdb441397e61dcd07a11f4d |
| Source note | uspto-grants-1983_09 |