HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzaldehyde → HCID 21496062, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Ethanone, 1-(4-amino-2-methyl-5-(2-methylphenyl)-1H-pyrrol-3-yl)- | HCID 41888 | — |
| Product | HCID 21496062 | HCID 21496062 | — |
Reaction Steps
The title compound (M.p. 167°-70° C) is prepared from 4-acetyl-3-amino-5-methyl-2-(o-tolyl)-pyrrole (m.p. 258° C), obtained substantially in the same way as compound A), by transforming into the corresponding p-chlorobenzylidene derivative (m.p. 215° C) by reaction with p-chlorobenzaldehyde and subsequent catalytic hydrogenation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03993650 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-c57b60805db44a8b93edaa7e005a407c |
| Source note | uspto-grants-1976_11 |