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Chemical Structure| 54523-24-9 Chemical Structure| 54523-24-9

Structure of 54523-24-9

Chemical Structure| 54523-24-9

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Product Details of [ 54523-24-9 ]

CAS No. :54523-24-9
Formula : C29H18Br2O
M.W : 542.26
SMILES Code : O=C1C(C2=CC=C(Br)C=C2)=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=C1C5=CC=C(Br)C=C5
MDL No. :MFCD32062867

Safety of [ 54523-24-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 54523-24-9 ]

* 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 [ 54523-24-9 ]

[ 54523-24-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 54523-47-6 ]
  • [ 134-81-6 ]
  • [ 54523-24-9 ]
YieldReaction ConditionsOperation in experiment
91% With potassium hydroxide; In methanol; dichloromethane; for 1.5h;Inert atmosphere; Reflux; To a solution of <strong>[54523-47-6]1,3-bis(4-bromophenyl)-2-propanone</strong> (3 300 mg, 0.815 mmol) and benzyl (0.815 mmol) in dichloromethane (1.5 mL)(30 mL) was added potassium hydroxide (22.8 mg, 0.407 mmol) as a solution in methanol (3 mL). the reaction was heated to reflux under nitrogen for 90 minutes before cooling in an ice bath. This mixture was introduced into 50 mL of cold methanol, and the obtained solid 2,5-bis(4-bromophenyl)-3,4-diphenylcyclopenta-2,4-dienone (4) was filtered to obtain a dark purple solid (404 mg, 91% yield).
68% After benzyl (1.14 g, 5.4 mmol) and di(4-bromophenyl)acetone (2.0 g, 5.4 mmol) were dissolved in 40 mL of ethanol and heated, the mixture was refluxed under stirring <n="34"/>for 1 hour. KOH (0.3 g, 5.4 mmol) dissolved in 10 mL of ethanol was slowly added drop wise thereto, and then refluxed under stirring for 30 minutes. The resultant was slowly cooled to give a dark red solid powder. The obtained dark red solid powder was filtered under reduced pressure, and then dried under vacuum to obtain a starting material represented by Formula i.[104] (2.0 g, 68 %); 1H NMR (400 MHz, DMSO-J ) 7.50-7.48(d, 4H), 7.30-7.23(m, 6H),7.11-7.09(d, 4H), 6.98-6.96(d, 4H) ; MS [M+H] 540,542,544
 

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