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Methanol → Quino[2,3-b]acridine-7,14-dione, 2,9-dichloro-5,12-dihydro-

HRID 861200
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 861200
[Cl:1][C:2]1[CH:28]=[CH:27][C:5]([NH:6][C:7]2[CH:15]=[C:14]([C:16]([OH:18])=O)[C:13]([NH:19][C:20]3[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=3)=[CH:12][C:8]=2[C:9]([OH:11])=O)=[CH:4][CH:3]=1.P(=O)(O)(O)O.CO>O.C(NN(NCC)S(C1C2=C3C(C4C5C(=CC=CC2=5)C=CC=4)=CC=CC3=CC=1CCC)(=O)=O)C>[CH:3]1[C:2]([Cl:1])=[CH:28][C:27]2[C:9]([C:8]3[C:7]([NH:6][C:5]=2[CH:4]=1)=[CH:15][C:14]1[C:16]([C:21]2[CH:22]=[C:23]([Cl:26])[CH:24]=[CH:25][C:20]=2[NH:19][C:13]=1[CH:12]=3)=[O:18])=[O:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 887MethanolHCID 1004Phosphoric AcidHCID 1705571,4-Benzenedicarboxylic acid, 2,5-bis[(4-chlorophenyl)amino]-

Produkt 1

HCID 76530Quino[2,3-b]acridine-7,14-dione, 2,9-dichloro-5,12-dihydro-Ausbeute 96,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 131720450
n,n-Diethylaminopropyl perylenesulfonamide
Katalysator
HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
113 °C

Versuchsvorschrift

To 300 g of polyphosphoric acid (117% phosphoric acid) heated at 80° C. was added 5 g N,N-diethylaminopropyl perylenesulfonamide followed by 50 g of 2,5-di(4-chloroanilino)terephthalic acid added over a period of 40 minutes, the temperature being maintained below 110° C. by adjustment of the addition rate. The mixture was heated at 113° C. for 4.5 hours. After the melt was cooled to 97° C., the acid strength was adjusted to 111% by the dropwise addition of phosphoric acid. The resultant melt was slowly poured into 525 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 presscake was dried to obtain 44.1 g of crude dichloroquinacridone, which was then salt ground for three hours using 306 g of a microsized salt and 54.9 g of a glycol. The salt was extracted using a slightly alkaline water slurry at 65° C. for one hour. After the slurry was filtered, the presscake was reslurried in slightly acidic water and held at 65° C. for one hour. The solid component was collected by filtration and washed with water. The wet cake can be dried or used as is for specific applications. Here, the wet cake was dried in an oven at 60° C. to give approximately 44 g of 2,9-dichloroquinacridone as a magenta pigment.

Aufarbeitung

  1. additionadded over a period of 40 minutes
  2. temperaturethe temperature being maintained below 110° C. by adjustment of the addition rate
  3. temperatureAfter the melt was cooled to 97° C.
  4. temperaturethe temperature being maintained below 64° C.
  5. temperatureby external cooling
  6. additionadjustment of melt addition rate
  7. temperatureThe slurry was heated
  8. temperatureat reflux for one hour
  9. temperaturecooled to below 60° C.
  10. filtrationfiltered
  11. washwashed until acid free
  12. customThe presscake was dried
  13. customto obtain 44.1 g of crude dichloroquinacridone, which
  14. extractionThe salt was extracted
  15. customat 65° C.
  16. customfor one hour
  17. filtrationAfter the slurry was filtered
  18. waitheld at 65° C. for one hour
  19. filtrationThe solid component was collected by filtration
  20. washwashed with water
  21. customThe wet cake can be dried
  22. customHere, the wet cake was dried in an oven at 60° C.

Quellen und Nachweise

ORD-Eintrag
ord-8e19e068189c4584a886ed43e15520a7
Quelldatensatz
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05713999

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