HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetanilide → HCID 23094067, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetanilide | HCID 904 | — |
| Reactant | 1,4-Dibromo-2-nitrobenzene | HCID 77004 | — |
| Product | HCID 23094067 | HCID 23094067 | 61% |
Reaction Steps
The title compound was prepared with the analogous procedure described in example 1 using 2,5-Dibromonitrobenzene (140 mg, 0.5 mmol) and N-phenylacetamide (81 mg, 0.6 mmol) as starting materials to yield the title compound as a yellow solid (87 mg, 61%). 1H NMR (DMSO) δ 2.52 (s, 3 H), 7.18 (d, J=8.8 Hz, 1 H), 7.43 (d, J=8.8 Hz, 1 H), 7.58-7.68 (m, 5 H), 7.98 (br s, 1 H); 13C NMR δ 13.5, 112.5, 115.5, 119.5, 126.4, 126.9, 129.6, 130.1, 134.0, 139.0, 154.2, 156.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735586B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-4575540994c44f89a9991bceff60a734 |
| Source note | uspto-grants-2014_05 |