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[ CAS No. 16308-63-7 ] {[proInfo.proName]}

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Chemical Structure| 16308-63-7
Chemical Structure| 16308-63-7
Structure of 16308-63-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 16308-63-7 ]

CAS No. :16308-63-7 MDL No. :MFCD27578763
Formula : C22H18O4 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 346.38 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 16308-63-7 ]

* 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 [ 16308-63-7 ]

[ 16308-63-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 18014-00-1 ]
  • [ 98-80-6 ]
  • [ 16308-63-7 ]
YieldReaction ConditionsOperation in experiment
80% With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In water; toluene; for 8h;Heating / reflux; In a stream of argon, 35 g (0.1 mol) of <strong>[18014-00-1]methyl 2,5-dibromoterephthalate</strong>, 27 g (0.22 mol) of phenylboronic acid, 5.7 g (5 mmol) of tetrakistriphenylphosphinepalladium(0), 200 mL of toluene, and the mixture of 32 g (0.3 mol) of sodium carbonate and 150 mL of water were added to a 1-L three-necked flask, and the whole was refluxed under heat for 8 hours. After the completion of the reaction, an organic layer was washed with water and dried with magnesium sulfate, and then the solvent was removed by distillation with a rotary evaporator. The resultant coarse crystal was recrystallized with ethanol, whereby 27 g of Intermediate 1 (white crystal, 80% yield) as a target were obtained.
80% With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In water; toluene; for 8h;Reflux; Inert atmosphere; Synthesis Example 1(101) Synthesis of Intermediate 1; Into a 1 liter three-necked flask, 35 g (0.1 mole) of <strong>[18014-00-1]di<strong>[18014-00-1]methyl 2,5-dibromoterephthalate</strong></strong>, 27 g (0.22 moles) of phenyl boronic acid, 5.7 g (5 mmole) of tetrakis(triphenylphosphine)palladium(0), 200 ml of toluene and a solution prepared by dissolving 32 g (0.3 moles) of sodium carbonate into 150 ml of water were placed under the stream of argon, and the resultant mixture was heated under the refluxing condition for 8 hours. After the reaction was completed, the organic layer was washed with water and dried with magnesium sulfate, and the solvent was removed by distillation using a rotary evaporator. The obtained crude crystals were recrystallized from ethanol, and 27 g of Intermediate 1 of the object compound was obtained (white crystals; the yield: 80%).
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