HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 46198774, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 44814403 | HCID 44814403 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 46198774 | HCID 46198774 | 90% |
Reaction Steps
A suspension of 5-(4-benzoylpiperazin-1-yl)-2-nitro-N-phenylbenzenamine (1.0 g, 2.5 mmol), benzylbromide (0.3 ml, 2.5 mmol), potassium hydroxide (0.18 g, 3.2 mmol) and tetra-butyl ammonium iodide (0.05 g, 0.25 mmol) in 40 ml toluene was stirred at room temperature overnight. The red solids were filtered to get N-benzyl-5-(4-benzoylpiperazin-1-yl)-2-nitro-N-phenylbenzenamine (1.1 g, 90%). 1H NMR (500 MHz, DMSO-d6) δ (ppm) 3.40-3.58 (m, br, 8H), 4.94 (s, 2H), 6.30 (d, J=8.0 Hz, 2H), 6.73 (t, J=7.2 Hz, 1H), 6.88 (d, J=9.2 Hz, 2H), 7.09-7.48 (m, 12H), 7.98 (d, J=8.9 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420640B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-3831fd5349ef4df0a8394682f1676da3 |
| Source note | uspto-grants-2013_04 |