HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminobiphenyl → 2-(o-Biphenylyl)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminobiphenyl | HCID 7015 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Butyl nitrite | HCID 10996 | — |
| Product | 2-(o-Biphenylyl)thiophene | HCID 14243986 | 34.8% |
Reaction Steps
In a 4-l Erlenmeyer flask were placed 100 g (0.600 mole) of Pfalz and Bauer o-aminobiphenyl, m.p. 49°-51° C., 3000 ml (38.2 moles) of thiophene and 90 ml (0.80 mole) of n-butyl nitrite. The mixture was thoroughly stirred and then allowed to stand at room temperature for eight days. Unreacted thiophene was removed by distillation. The residue was distilled at reduced pressure to give 49.4 g (34.8%) of 2-(o-biphenylyl)thiophene b.p. 138°-155° C. (0.1 mm), ND20 1.6465.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174405 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-eccd3d4c1897434e80a4312eac06faaf |
| Source note | uspto-grants-1979_11 |