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Chemical Structure| 1337916-18-3 Chemical Structure| 1337916-18-3

Structure of 1337916-18-3

Chemical Structure| 1337916-18-3

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Product Details of [ 1337916-18-3 ]

CAS No. :1337916-18-3
Formula : C10H8BBrO2
M.W : 250.88
SMILES Code : BrC1=CC2=CC=C(B(O)O)C=C2C=C1
MDL No. :MFCD18410711
InChI Key :JOSJENCQBZHUDM-UHFFFAOYSA-N
Pubchem ID :58461093

Safety of [ 1337916-18-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1337916-18-3 ]

* 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 [ 1337916-18-3 ]

[ 1337916-18-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 689291-89-2 ]
  • [ 1337916-18-3 ]
  • 5-bromo-2-(6-bromo-2-naphthalenyl)benzaldehyde [ No CAS ]
YieldReaction ConditionsOperation in experiment
90% With tetrakis(triphenylphosphine) palladium(0); caesium carbonate; In ethanol; water; toluene; at 90℃; for 24h; A mixed solution of toluene (80 mL), ethanol (40 mL), 2M Cs2CO3 aqueous solution (80 mL) in a 500 ml two-necked flask was added for 30 minutes, and then added.<strong>[689291-89-2]5-bromo-2-iodobenzaldehyde</strong> (3.10 g, 10 mmol),With 6-bromo-2-naphthalene boronic acid (2.8 g, 11 mmol),Pd(PPh3)4 (230 mg, 0.2 mmol).Stir for 24 hours by heating to 90 C.Extracted with dichloromethane, washed with water, dried over anhydrous sodium sulfate and filtered.After concentration, 3.5 g of the product was obtained by column chromatography, yield 90%.
82% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; water; toluene; at 80℃; for 24h;Sonication; Into a 500ml two-necked flask feed toluene (80mL), ethanol (40mL), 2Μ K2C03 aqueous solution (80mL) mixed solution for 30 minutes after ultrasonication added <strong>[689291-89-2]5-bromo-2-iodobenzaldehyde</strong> (3.10g, 10mmol), with 6-bromo-2-naphthaleneboronic acid (2.8g, 11mmol), Pd(PPh3) 4 (230 mg, 0.2mmol). Heat at 80 C for 24 hours, extract with dichloromethane, and wash with water, dry with anhydrous sodium sulfate, filtered, concentrated and passed through column chromatography and then obtained product 3.2g, yield 82%.
 

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