HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitro-2-phenylthiophene → 2-Phenylthiophen-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitro-2-phenylthiophene | HCID 18925396 | — |
| Reactant | HCID 18925402 | HCID 18925402 | — |
| Product | 2-Phenylthiophen-3-amine | HCID 18925395 | 81% |
Reaction Steps
The same procedures as described in Example 3 were carried out except that 3-nitro-2-(4-chlorophenyl)thiophene was replaced by 3-nitro-2-phenylthiophene. The yield was 81%. 1H-NMR(CDCl3, δ value):3.82(2H, brs), 6.66(1H, d, J=5.1), 7.12(1H, d, J=5.1), 7.22-7.29(1H, m), 7.42(2H, dt, J=1.5, 7.3), 7.52(2H, dd, J=1.5, 7.3)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05747518 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-76c78543a953450d946f163bb0b939a2 |
| Source note | uspto-grants-1998_05 |