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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287183Generated: October 25, 2026

1-Chloro-2,6-dinitrobenzene → 4-(2,6-Dinitrobenzylidene)-1-ethyl-1,4-dihydroquinoline

https://huagongshe.com/reaction/1287183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2,6-dinitrobenzeneHCID 11814—
ReactantQuinolinium, 1-ethyl-4-methyl-, iodide (1:1)HCID 69062—
ReactantDiisopropylethylamineHCID 81531—
SolventAcetonitrileHCID 6342—
Product4-(2,6-Dinitrobenzylidene)-1-ethyl-1,4-dihydroquinolineHCID 5401220425%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03984248
Source datasetuspto-grants-1976_10
ORD IDord-33af87ddf59c451298e3aab5131f534e
Source noteuspto-grants-1976_10