HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-2,6-dinitrobenzene → 4-(2,6-Dinitrobenzylidene)-1-ethyl-1,4-dihydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-2,6-dinitrobenzene | HCID 11814 | — |
| Reactant | Quinolinium, 1-ethyl-4-methyl-, iodide (1:1) | HCID 69062 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(2,6-Dinitrobenzylidene)-1-ethyl-1,4-dihydroquinoline | HCID 54012204 | 25% |
Reaction Steps
1-Ethyllepidinium iodide (3.0 g., 10 mmole) and 1-chloro-2,6-dinitrobenzene (2.5 g., 12 mmole) are warmed in acetonitrile (50 ml.) and diisopropylethylamine (2.6 g., 20 mmole) is added. The resulting dark mixture is allowed to cool and stand overnight. The precipitate of dye is filtered off and washed with acetonitrile and ether. On recrystallization from acetonitrile, a 25% yield (0.85 g.) of purified dye is obtained with a m.p. of 154°-155° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03988154 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-041ebbf1bff34b118f1794e6a753fd95 |
| Source note | uspto-grants-1976_10 |