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

HRID 861198
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HRID 861198 반응식
[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]
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참가 물질

6

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

생성물 1

HCID 76530Quino[2,3-b]acridine-7,14-dione, 2,9-dichloro-5,12-dihydro-수율 94.1%

시약·촉매·용매 2

HCID 131720450n,n-Diethylaminopropyl perylenesulfonamide촉매
HCID 962
Water
용매

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온도
113 °C

실험 절차

To 300 g of polyphosphoric acid (117% phosphoric acid) heated at 80° C. was added 0.5 g N,N-diethylaminopropyl perylenesulfonamide (prepared according to U.S. Pat. No. 4,310,359) 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 92° 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 43.8 g of crude dichloroquinacridone, which was then salt ground for three hours using 306 g of a microsized salt and 54.6 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 43 g of 2,9-dichloroquinacridone as a magenta pigment.

후처리

  1. customprepared
  2. additionadded over a period of 40 minutes
  3. temperaturethe temperature being maintained below 110° C. by adjustment of the addition rate
  4. temperatureAfter the melt was cooled to 92° C.
  5. temperaturethe temperature being maintained below 64° C.
  6. temperatureby external cooling
  7. additionadjustment of melt addition rate
  8. temperatureThe slurry was heated
  9. temperatureat reflux for one hour
  10. temperaturecooled to below 60° C.
  11. filtrationfiltered
  12. washwashed until acid free
  13. customThe presscake was dried
  14. customto obtain 43.8 g of crude dichloroquinacridone, which
  15. extractionThe salt was extracted
  16. customat 65° C.
  17. customfor one hour
  18. filtrationAfter the slurry was filtered
  19. waitheld at 65° C. for one hour
  20. filtrationThe solid component was collected by filtration
  21. washwashed with water
  22. customThe wet cake can be dried
  23. customHere, the wet cake was dried in an oven at 60° C.

출처 및 근거

ORD 기록
ord-2570cd4038db451ca5209acba541dea7
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05713999

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