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Chemical Structure| 82531-03-1

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Product Details of [ 82531-03-1 ]

CAS No. :82531-03-1
Formula : C40H42N2O4
M.W : 614.77
SMILES Code : O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(CC(CC)CCCC)C(C5=CC=C6C3=C54)=O)=O)C7=C6C=CC1=C27)=O

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Application In Synthesis of [ 82531-03-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 82531-03-1 ]

[ 82531-03-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 82531-03-1 ]
  • [ 851786-15-7 ]
YieldReaction ConditionsOperation in experiment
41.86% With bromine; In dichloromethane; at 50℃; for 48h; (1) Synthesis of PBI-2Br molecule: Dissolve N, N-diisooctylamino-perylene diimide (10mmol, 6.15g) in 150mL of CH2Cl2 and slowly add 34mL Br2, stir at 50 C-cool to reflux for 48h,Remove the flask from the oil bath and wait for the reaction to reach room temperature, then pour the reaction solution into a 1000mL beaker.5 g of sodium thiosulfate was added to the mixture system and stirred overnight to remove unreacted bromine,After that, the mixture was vacuum filtered and washed three times with ultrapure water to obtain a dark red solid powder, which was dried in a vacuum drying oven at 50 C for 5 hours.Dissolve the crude brominated PBI product with dichloromethane, add silica gel to prepare the sample, and dissolve the crude brominated PBI product with dichloromethane.Add silica gel to mix sample, and separate by multiple times through column chromatography to obtain perylene diimide dibromide PBI-2Br (0.72g, 41.86%).
6.57 g With bromine; In dichloromethane; at 50℃; for 24h; 3,4,9,10-perylene bisanhydride (1, 3.82 g, 10 mmol) and 2-ethylhexylamine (12.9 g, 100 mmol) were mixed with 100 mL pyridine. The resulted mixture was allowed to react under reflux for 2 days. Then, the mixture was poured into 1M hydrochloric acid aqueous solution (1 L) and the resulted red solid was filtered to give crude product (2). With further purification, 2 was dissolved into 500 mL of dichloromethane (DCM). To which 20 mL bromine was dropwise added. After addition of bromine, the mixture was then allowed to react for another 24 hours. The excess of bromine was removed by flow of N2 and the red solid was applied to chromatography with petroleum ether (60-90C) /DCM=1:10 as eluents to afford product (3) in a yield of 85% (6.57 g). 1H-NMR (400MHz, CDCl3) d ppm: 9.38 (d, J = 8.00 Hz, 2H), 8.81 (s, 2H), 8.60 (d, J = 8.00 Hz, 2H), 4.12 (m, J = 12.92 Hz, 8.00 Hz, 5.96 Hz, 12.92 Hz, 4H), 1.93 (s, 2H), 1.40 (m, J = 6.00 Hz, 6.40 Hz, 8H), 1.32 (m, J = 6.00 Hz, 4.00 Hz, 8H), 0.96 (m, J = 6.20 Hz, 2.80 Hz, 6H), 0.91 (m, J = 10.80 Hz, 5.20 Hz, 6H). 13C-NMR (100 MHz, CDCl3) d ppm: 163.6, 163.2, 162.7, 162.4, 138.2, 138.1, 133.1, 132.8, 132.7, 132.3, 130.1, 129.9, 129.2, 128.5, 128.1, 127.0, 123.4, 123.2, 122.8, 121.5, 121.7, 120.9, 44.6, 38.1, 30.9, 28.8, 24.2, 23.2, 14.2, 10.8. TOF MS: m/z = 773.1 [M+H]+.
With bromine; In dichloromethane;Reflux; The product is used without any treatment, was dissolved in 100mL of dichloromethane, heating under reflux, was added dropwise to 20mL of elemental bromine addition was completed, heating was continued at reflux overnight. Through a silica gel column with H60 to give the product 3.
  • 2
  • [ 82531-03-1 ]
  • [ 851786-15-7 ]
  • [ 1015473-19-4 ]
  • 3
  • [ 82531-03-1 ]
  • [ 851786-15-7 ]
  • N,N'-bis(2-ethylhexyl)-1,6-dibromoperylene-3,4:9,10-tetracarboxylic acid diimide [ No CAS ]
 

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