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Chemical Structure| 49764-92-3 Chemical Structure| 49764-92-3

Structure of 49764-92-3

Chemical Structure| 49764-92-3

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Product Details of [ 49764-92-3 ]

CAS No. :49764-92-3
Formula : C29H16Br4O
M.W : 700.05
SMILES Code : O=C1C(C2=CC=C(Br)C=C2)=C(C3=CC=C(Br)C=C3)C(C4=CC=C(Br)C=C4)=C1C5=CC=C(Br)C=C5
MDL No. :N/A

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Application In Synthesis of [ 49764-92-3 ]

* 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 [ 49764-92-3 ]

[ 49764-92-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35578-47-3 ]
  • [ 54523-47-6 ]
  • [ 49764-92-3 ]
YieldReaction ConditionsOperation in experiment
68% With potassium hydroxide; In ethanol; dichloromethane; water; Preparative Example 11 2,3,4,5-Tetra(4-bromophenyl)cyclopentadienone (14) A solution of potassium hydroxide (230 mg, 4.1 mmol) in ethanol (5 cm3) was added to a solution of (13) (3.01 g, 8.2 mmol) and 4,4'-dibromobenzil (3.01 g, 8.2 mmol) in ethanol (45 cm3) at 70 C., and the reaction was stirred at 70 C. for 4 hours. Water (200 cm3) and dichloromethane (200 cm3) were added, and the layers were separated. The organic layer was washed with brine (200 cm3) and dried over magnesium sulfate. The solvent was removed to leave a dark purple solid. The crude product was passed through a plug of silica, and then recrystallized from a dichloromethane/ethanol mixture to give (14) as a dark purple crystalline solid (3.87 g, 68%).
62% With potassium hydroxide; In ethanol; for 0.666667h;Reflux; To a solution of 056 (310 mg, 0.84 mmol, 1 equiv) and 101 (310 mg, 0.84 mmol, 1 equiv) in ethanol (3 mL) was added a solution of KOH (47 mg, 0.84 mmol, 1 equiv) in ethanol (0.5 mL). The reaction mixture was stirred at reflux for 40 mm. The dark redsolution was then cooled down to 0 00. The resulting dark red precipitate was filtered and washed with cold ethanol, affording 102 as dark red crystals (365 mg, 62 %).
After 4,4v-dibromobenzyl (9.8 g, 27 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 for 1 hour. KOH (0.3 g, 5.4 mmol) dissolved in 10 mL of ethanol was slowly added dropwise 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 <n="35"/>solid powder was filtered under reduced pressure, and then dried under vacuum to obtain a starting material represented by Formula k. [114] MS [M+H] 700
 

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