HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzyl bromide → 2-Butyl-4,5-dicyano-1-(4-nitrobenzyl)imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | 2-butyl-1H-imidazole-4,5-dicarbonitrile | HCID 5260591 | — |
| Product | 2-Butyl-4,5-dicyano-1-(4-nitrobenzyl)imidazole | HCID 19815389 | — |
Reaction Steps
2-n-Butyl-4,5-dicyano-1-(4-nitrobenzyl)imidazole was prepared from 2-n-butyl-4,5-dicyanoimidazole by the procedure in Example 1, Part A using 4-nitrobenzyl bromide as the alkylating agent. The product was obtained as an oil. NMR (200 MHz, CDCl3) δ 8.29 (d, 2H, J=10 Hz); 7.29 (d, 2H, J=10 Hz); 5.36 (s, 2H); 2.67 (t, 2H, J=7 Hz); 1.70 (t of t, 2H, J=7,7 Hz); 1.36 (t of q, 2H, J=7,7 Hz); 0.86 (t, 3H, J=7 Hz); Mass Calcd. for C16H15N5O2 : 309.1225. Found: 309.1211.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155118 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-00c38bd405d748d88c5874f950ec6ec1 |
| Source note | uspto-grants-1992_10 |