HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-imidazole-2-carbaldehyde → 1-(o-Nitrobenzyl)-imidazole-2-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-imidazole-2-carbaldehyde | HCID 24955 | — |
| Reactant | alpha-Bromo-2-nitrotoluene | HCID 77569 | — |
| Product | 1-(o-Nitrobenzyl)-imidazole-2-carboxaldehyde | HCID 12724985 | 94.4% |
Reaction Steps
With stirring and external cooling, 4.80 g of 2-imidazolecarboxaldehyde is added and the cooling bath removed. Slight external heating results in a yellow solution. The reaction mixture is chilled in ice and 10.8 g of 2-nitrobenzyl bromide is added. The reaction mixture is stirred at 0° C. for 18 hours. The volatiles are removed in vacuo to a residue which is stirred with ice water, filtered and the cake washed well with water and suction dried to give 10.9 g of the desired product as a solid, m.p. 141-144° C. MH+ 232.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05968930 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-4a8d2014e5944140aa808f5bdf64101a |
| Source note | uspto-grants-1999_10 |