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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078536Generated: November 3, 2026

1-Chloronaphthalene → HCID 21280681, compound

https://huagongshe.com/reaction/1078536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ChloronaphthaleneHCID 7003—
ReactantO-PhenylenediamineHCID 7243—
ProductHCID 21280681HCID 21280681—

Reaction Steps

39.2 g of perylene-3,4,9,10-tetracarboxylic acid dianhydride, 32.4 g of o-phenylenediamine and 800 ml of α-chloronaphthalene were mixed, and the mixture was reacted at 260° C. for 6 hours. After the reaction product was left to cool, deposited crystals were collected by filtration, and were then repeatedly washed with methanol, followed by heating and drying to obtain 51.1 g of an imidazole perylene compound as a mixture of the compounds of Structural formulas 1 and 2. The product thus obtained was called a synthesized product, whose X-ray diffraction spectrum was as shown in FIG. 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05549997
Source datasetuspto-grants-1996_08
ORD IDord-a546c20daa0c4e68bb12df6b8e4e98ce
Source noteuspto-grants-1996_08