HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 3-Chloro-2-methylbiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 3-Chloro-2-methylaniline | HCID 6894 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Product | 3-Chloro-2-methylbiphenyl | HCID 4601832 | — |
Reaction Steps
Under a dry nitrogen atmosphere isoamyl nitrite (37 grams, 0.31 mole) was added to a stirred solution of 3-chloro-2-methylaniline (35 grams, 0.25 mole) in benzene (500 ml). The mixture was heated at reflux for 1.5 hours, then allowed to cool and stirred at 50° for approximately 18 hours. The reaction mixture was cooled to room temperature, then evaporated under reduced pressure to a red residue. The residue was distilled under reduced pressure to give a yellow oil (bp 115°-130°/0.9 mm). The pot residue was washed with chloroform and the distillate dissolved in chloroform. The chloroform fractions were combined, washed with 10% aqueous hydrochloric acid and evaporated to give 3-chloro-2-methyl[1,1'-biphenyl] as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04507317 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-ad21f74f0492431d84179a4cf824fe3d |
| Source note | uspto-grants-1985_03 |