HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 85845687, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 85845685 | HCID 85845685 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 85845687 | HCID 85845687 | — |
Reaction Steps
The hydrazones formed in this manner are in turn allowed to react with N-bromosuccinimide at about room temperature in a suitable solvent, such as chloroform, to yield 1-methyl-5-nitroimidazole-2-carbonyl bromide alkyl or hydroxy-alkyl hydrazones. The reaction with N-bromosuccinimide is applicable to any of the substituted hydrazones to yield the bromo-substituted hydrazones. As a specific example, when 1-methyl-5-nitroimidazole-2-carboxaldehyde methyl hydrazone is allowed to react with N-bromosuccinimide at room temperature in chloroform solvent, there is obtained 1-methyl-5-nitroimidazole-2-carbonyl bromide methyl hydrazone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075222 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-844331161d40437dba0c8c971ed5b19d |
| Source note | uspto-grants-1978_02 |