HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Hexanedione → 4-(2,5-Dimethyl-1H-pyrrol-1-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Hexanedione | HCID 8035 | — |
| Reactant | 4-Aminobenzaldehyde | HCID 11158 | — |
| Reactant | HCID 86745551 | HCID 86745551 | — |
| Product | 4-(2,5-Dimethyl-1H-pyrrol-1-yl)benzaldehyde | HCID 2764550 | — |
Reaction Steps
Similarly prepared is N-acetyl-N-acetyloxy-[4-(2,5-dimethyl-1H-pyrrol-1-yl)-cinnamylamine. The starting material is prepared by first condensing p-amino-benzaldehyde with acetonylacetone to obtain 4-(2,5-di-methyl-1H-pyrrol-1-yl)-benzaldehyde which is in turn condensed with diethyl phosphonoacetaldehyde diethylacetal to obtain 4-(2,5-dimethyl-1H-pyrrol-1-yl)-cinnamaldehyde. The aldehyde is then converted to the oxime and reduced to the hydroxylamine according to previously described procedures.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05096919 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-d3a8c64b060b446c8f7641059b17090b |
| Source note | uspto-grants-1992_03 |