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Chemical Structure| 779-03-3 Chemical Structure| 779-03-3

Structure of 779-03-3

Chemical Structure| 779-03-3

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Product Details of [ 779-03-3 ]

CAS No. :779-03-3
Formula : C14H11N
M.W : 193.24
SMILES Code : NC1=C2C=CC=CC2=CC2=C1C=CC=C2
MDL No. :MFCD00452690
InChI Key :LHNICELDCMPPDE-UHFFFAOYSA-N
Pubchem ID :13069

Safety of [ 779-03-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 779-03-3 ]

* 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 [ 779-03-3 ]

[ 779-03-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4981-66-2 ]
  • [ 779-03-3 ]
  • 2
  • [ 108-86-1 ]
  • [ 779-03-3 ]
  • [ 15424-38-1 ]
YieldReaction ConditionsOperation in experiment
80% With tri-tert-butyl phosphine; palladium diacetate; sodium t-butanolate; In toluene; for 2h;Reflux; The tri-butyl phosphine (4.4 ml of 1.0M toluene solution, 1.48g, 0 . 05mmol), palladium acetate (0.4g, 1 . 83mmol) butyl sodium (22.8g, 238mmol) added to the 9 - amino anthracene (35.3g, 183mmol) and bromobenzene (59.9g, 183mmol) in degassing toluene (500 ml) of the solution in a, and the mixture is heated to reflux 2 hours. The reaction mixture is cooled to room temperature, the toluene dilution and for via the diatomaceous earth filter. The filtrate diluted with water, and is extracted with toluene, and combined with the organic phase, and under the condition of vacuum evaporation. The residue through silica gel (heptane/dichloromethane) filter, and from the isopropanol in crystallization. To obtain 1 - 4 (39.3g, the theoretical value of 80%).
80% With tri-tert-butyl phosphine; palladium diacetate; sodium t-butanolate; In toluene; for 2h;Reflux; A solution of tri-tert-butylphosphine (4.4 mL of 1.0 M in toluene, 1.48 g, 0.05 mmol)Palladium acetate (0.4 g, 1.83 mmol)And sodium tert-butoxide (22.8 g, 238 mmol)Was added to 9-aminanthracene (35.3 g, 183 mmol)And bromobenzene (59.9 g, 183 mmol)In degassed toluene (500 mL)And the mixture was heated under reflux for 2 hours.The reaction mixture was cooled to room temperature,Diluted with toluene and filtered through diatomaceous earth.The filtrate was diluted with water,And extracted with toluene,And the organic phase is combined,It was evaporated under vacuum.The residue was filtered through silica gel (heptane / dichloromethane)And crystallized from isopropanol.A2 (39.3 g, 80% theoretical).
 

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