HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloroaniline → HCID 13090793, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloroaniline | HCID 11123 | — |
| Reactant | HCID 13090835 | HCID 13090835 | — |
| Product | HCID 13090793 | HCID 13090793 | — |
Reaction Steps
20 parts of 3,5-dichloroquinoline-8-carbaldehyde (prepared by a method similar to that in Example 4) and 14.6 parts of 2,4-dichloroaniline in 300 parts of alcohol were refluxed for 3 hours. The solution was cooled and the precipitated product was filtered off with suction and recrystallized from methylglycol. 30 g of 3,5-dichloro-8-(2,4-dichlorophenyliminomethyl)-quinoline of melting point 156° C. were obtained. The yield corresponds to 90% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04632696 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-ae3fa0e2ee5a4069b082b4033bf6c4ae |
| Source note | uspto-grants-1986_12 |