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1-Chloronaphthalene → Benzimidazole perylene

HRID 1109701
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HRID 1109701 반응식
Cl[C:2]1C2C(=CC=CC=2)C=CC=1.[CH:12]1[C:21]2[C:22]3[CH:31]=[CH:30][C:29]4C(OC(=O)[C:27]5[C:28]=4[C:23]=3[C:24](=[CH:25][CH:26]=5)[C:19]3[C:20]=2[C:15]2[C:16](C(OC(=O)[C:14]=2[CH:13]=1)=O)=[CH:17][CH:18]=3)=O.[C:42]1([NH2:49])[CH:47]=[CH:46][CH:45]=[CH:44][C:43]=1[NH2:48].[OH-].[Na+]>CO.O>[CH:25]1[C:24]2=[C:23]3[C:22]([C:21]4[C:20]5[C:15](=[CH:16][CH:17]=[CH:18][C:19]2=5)[CH:14]=[CH:13][CH:12]=4)=[CH:31][CH:30]=[CH:29][C:28]3=[CH:27][CH:26]=1.[N:48]1[C:43]2[CH:44]=[CH:45][CH:46]=[CH:47][C:42]=2[NH:49][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 70031-ChloronaphthaleneHCID 7243O-PhenylenediamineHCID 14798Sodium HydroxideHCID 671913,4,9,10-Perylenetetracarboxylic dianhydride

생성물 1

HCID 21910037Benzimidazole perylene

시약·촉매·용매 2

HCID 887Methanol용매
HCID 962
Water
용매

실험 절차

78.7 Parts of 1-chloronaphthalene, 4.3 parts of perylene-3,4:9,10-tetracarboxylic dianhydride and 11.9 parts of o-phenylenediamine were charged in a stainless steel reactor equipped with a pitched blade turbine agitator, a circulation jacket connected to an oil supply system, a temperature measuring element and a distillation line with a condenser. After the aforementioned raw materials were charged and the agitator speed adjusted to 200 rpm, the reactor was purged with nitrogen gas, and the reactor contents were heated by raising the temperature of the jacket in about one hour to the desired reaction temperature of 240° to 245° C. The reaction was continued for an additional 6 hours at this temperature. The reactor was then cooled by cooling the jacket oil with water to about 90° C. and the reactor contents were then transferred to a Nutsche vacuum filter equipped with an agitator. The filtrate was drained by applying vacuum to the filter. The crude, wet pigment cake was reslurry washed twice using 80 parts of warm dimethylformamide, with the wash filtrate drained each time by vacuum filtration. The cake was subsequently reslurry washed nine times with alkaline methanol at room temperature to, for example, remove acidic impurities. Each alkaline methanol wash was prepared by dissolving 0.33 part of sodium hydroxide in 66 parts of methanol. The pigment cake was then reslurry washed four times with methanol (66 parts of methanol used in each wash) and dried in a vacuum dryer at 65° C. and full vacuum for 16 hours. 5.89 Parts of crude benzimidazole perylene powder were obtained.

후처리

  1. customequipped with a pitched blade turbine agitator
  2. customthe reactor was purged with nitrogen gas
  3. temperaturethe reactor contents were heated
  4. temperatureby raising the temperature of the jacket in about one hour to the desired
  5. customreaction temperature of 240° to 245° C
  6. temperatureThe reactor was then cooled
  7. filtrationfilter
  8. customequipped with an agitator
  9. washwashed twice
  10. filtrationby vacuum filtration
  11. washThe cake was subsequently reslurry washed nine times with alkaline methanol at room temperature to, for example
  12. customremove acidic impurities
  13. washEach alkaline methanol wash
  14. customwas prepared
  15. washThe pigment cake was then reslurry washed four times with methanol (66 parts of methanol
  16. washeach wash) and
  17. customdried in a vacuum dryer at 65° C.
  18. waitfull vacuum for 16 hours

출처 및 근거

ORD 기록
ord-32363aa586fe43ff8edeacea3382b174
출처 데이터셋
uspto-grants-1994_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05322755

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