HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-BROMO-5-(4-METHYL-PIPERAZIN-1-YL)-BENZALDEHYDE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(4-Methylpiperazin-1-yl)benzaldehyde | HCID 26338804 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-BROMO-5-(4-METHYL-PIPERAZIN-1-YL)-BENZALDEHYDE | HCID 11403329 | 95% |
Reaction Steps
A solution of 3-(4-Methyl-piperazin-1-yl)-benzaldehyde (49 mmol) in methylene chloride (150 ml) was slowly (30 min) added a solution of N-bromosuccinimide (98 mmol) in methylene chloride (450 ml). The mixture was stirred for 10 min, washed with 2M sodium hydroxide and the organic phase was removed under reduced pressure. The resulting oil was purified by column chromatography giving the title compound as 90% pure black oil in 95% yield (the impurity being 4-bromo-3-(4-methyl-piperazin-1-yl)-benzaldehyde).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07642367B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-e5a84479f06b4807a0e9b1752f35876f |
| Source note | uspto-grants-2010_01 |