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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413330Generated: November 1, 2026

Hydrochloric Acid → Perylene

https://huagongshe.com/reaction/1413330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStearic AcidHCID 5281—
ReactantOctadecylamineHCID 15793—
ReactantHCID 86737471HCID 86737471—
SolventIsopropanolHCID 3776—
SolventPotassium HydroxideHCID 14797—
SolventPotassiumHCID 5462222—
SolventPerylene-1,2,3,4-tetracarboxylic acidHCID 19063515—
ProductPeryleneHCID 9142—

Reaction Steps

27.4 parts of crude perylenetetracarboxylic dianhydride in the form of the potassium salt of perylenetetracarboxylic acid are dissolved in aqueous potassium hydroxide solution as described in Example 1. To this solution are added 2 parts of stearic acid, dissolved in 60 parts by volume of 1% potassium hydroxide solution. With stirring, the alkaline perylenetetracarboxylic acid/stearic acid solution is added dropwise in the course of 15 minutes at 60° C. to a suspension consisting of 1.4 parts of MgCl2.6H2O, 0.7 parts of stearylamine, 35 parts by volume of about 37% aqueous hydrochloric acid and 60 parts by volume of isopropanol. The formation of the anhydride imide is brought to completion by stirring the acid suspension for 31/2 hours at reflux temperature. The red pigment suspension is then filtered at about 70° C. The filter cake is washed neutral with cold water and dried in a vacuum cabinet at 80° C., affording 29.8 parts of a perylene pigment with properties as good as those of the pigment of Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04250079
Source datasetuspto-grants-1981_02
ORD IDord-87b70f3364c44a2c930935bdf9f06233
Source noteuspto-grants-1981_02