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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861201Generated: October 30, 2026

Methanol → 5,12-Dihydro-2,9-dimethylquino(2,3-b)acridine-7,14-dione

https://huagongshe.com/reaction/861201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2,5-Di-p-toluidinoterephthalic acidHCID 82524—
SolventWaterHCID 962—
Product5,12-Dihydro-2,9-dimethylquino(2,3-b)acridine-7,14-dioneHCID 7042385.9%

Reaction Conditions

Temperature123 °C

Reaction Steps

To 300 g of polyphosphoric acid (112% phosphoric acid) heated at 88° C. was added 0.07 g of N-[3-(N,N-dimethylaminopropyl)] copper phthalocyanine sulfonamide followed by 68.2 g of 2,5-di(4-methylanilino)terephthalic acid added over a period of 35 minutes, the temperature being maintained below 120° C. by adjustment of the addition rate. The mixture was heated at 123° C. for two hours. After the melt was cooled to 93° C., it was slowly poured into 500 g of methanol, the temperature being maintained below 64° C. by external cooling and adjustment of melt addition rate. The slurry was heated at reflux for one hour, cooled to below 60° C., diluted with water, filtered, and washed until acid free. The resultant presscake was reslurried in water. After adjustment of the pH to greater than 7, 5.5 g of 50% sodium hydroxide was added and the resultant slurry was heated at 90° C. for one hour. The slurry was cooled, filtered, and washed with water until alkali free, then reslurried in water. After adjustment of the pH to 9.5, the slurry was heated at 143° C. for two hours in a closed system (e.g., a pressure reactor), and cooled to 40° C. After the slurry was acidified to pH 3.3, an emulsion of 2.2 g of an anionic surfactant, 30 g of a petroleum distillate, and 80 g of water was added, and the slurry was stirred for three hours. The solid component was collected by filtration and washed with water. The wet cake was dried in an oven at 60° C. to give approximately 53 g of 2,9-dimethylquinacridone as a magenta pigment.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05713999
Source datasetuspto-grants-1998_02
ORD IDord-0d517a2485134e238acf0e0b147c93aa
Source noteuspto-grants-1998_02