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[ CAS No. 1647102-86-0 ] {[proInfo.proName]}

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Chemical Structure| 1647102-86-0
Chemical Structure| 1647102-86-0
Structure of 1647102-86-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1647102-86-0 ]

CAS No. :1647102-86-0 MDL No. :
Formula : C12H13BO4 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 232.04 Pubchem ID :-
Synonyms :

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* 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 [ 1647102-86-0 ]

[ 1647102-86-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1647102-86-0 ]
  • [ 1206249-40-2 ]
  • [ 2415934-13-1 ]
YieldReaction ConditionsOperation in experiment
10.4 g With palladium diacetate; potassium carbonate; tris-(o-tolyl)phosphine In ethanol; water; toluene at 50℃; for 3h; Inert atmosphere; 1.3 Synthesis of 3,5-dichloro-2- (2-methoxymethoxynaphthalen-1-yl) pyrazine Next, about 26 g (used as 80 mmol) of the crude 2-methoxymethoxy-naphthalene-1-boronic acid obtained in Step 2 above and 18.23 g (80 mmol) of 2-bromo-3,5-dichloropyrazine were used. , 33.17 g (240 mmol) of potassium carbonate were placed in a 1 L three-necked flask, 400 mL of toluene, 135 mL of ethanol, and 120 mL of water were added, and then the inside of the flask was degassed under reduced pressure while stirring, Was replaced with nitrogen.Next, 179.61 mg (0.8 mmol) of palladium (II) acetate and 486.99 mg (1.6 mmol) of tris (2-methylphenyl) phosphine were added to this mixture, and then heated at 50 ° C. for 3 hours. It was stirred. After allowing to cool to room temperature, the reaction solution was extracted with toluene to obtain a black oily substance. After adding 50 mL of toluene to this black oily matter, the mixture was passed through a layer of Celite and alumina for purification to obtain a red solution. The red solution was concentrated to remove the solvent, hexane was added, recrystallization was performed at -10 ° C, and the precipitated solid was filtered off by suction filtration to obtain 10.40 g of a target brown solid, step. A total of two steps of 2, 3 was obtained with a yield of 38%. The synthetic scheme of Step 3 is shown in the following formula (a-3).
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