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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268308Generated: October 30, 2026

N-bromobutanimide → HCID 85845687, compound

https://huagongshe.com/reaction/268308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 85845685HCID 85845685—
SolventChloroformHCID 6212—
ProductHCID 85845687HCID 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 ini chloroform solvent, there is obtained 1 -methyl-5-nitroimidazole-2-carbonyl bromide methyl hydrazone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947467
Source datasetuspto-grants-1976_03
ORD IDord-1624fbbd27b04a4ab7dba55fb45cb2a4
Source noteuspto-grants-1976_03