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Chemical Structure| 851199-57-0 Chemical Structure| 851199-57-0

Structure of 851199-57-0

Chemical Structure| 851199-57-0

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Product Details of [ 851199-57-0 ]

CAS No. :851199-57-0
Formula : C12H8FIO
M.W : 314.09
SMILES Code : IC1=CC=C(OC2=CC=CC=C2F)C=C1
MDL No. :MFCD18207465

Safety of [ 851199-57-0 ]

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 [ 851199-57-0 ]

* 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 [ 851199-57-0 ]

[ 851199-57-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5419-55-6 ]
  • [ 851199-57-0 ]
  • [ 1402238-32-7 ]
YieldReaction ConditionsOperation in experiment
90% Step 4Into a 300 mL 3-necked round-bottom flask purged and maintained under an inert atmosphere of nitrogen, was placed a solution of l-(2-fluorophenoxy)-4-iodobenzene (3.3 g, 30.51 mmol, 1.00 equiv) in tetrahydrofuran (50 mL). n-BuLi (4.4 mL) was added dropwise with stirring at -78 C. The resulting solution was stirred for 10 mins at -78C and then tris(propan-2-yl)borate (2.1 g, 1 3.17 mmol, 1.06 equiv) was added dropwise with stirring at - 78 C over 30 min. The resulting solution was stirred while the temperature warmed from -78 C to room temperature. The reaction was then quenched by the addition of saturated aqueous NII4CI and concentrated under vacuum. The resulting solution was diluted with 30% aquious potassium hydroxide and then washed with ether. The pH of the aqueous was adjusted to 2-4 with hydrogen chloride (37% ). The resulting solution was extracted with ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum to give 2,2 g (90%) of [4-(2-fSuorophenoxy)phenyl]boronic acid as a white solid
90% Step 4 Into a 100 mL 3-necked round-bottom flask purged and maintained under an inert atmosphere of nitrogen, was placed a solution of 1-(2-fluorophenoxy)-4-iodobenzene (3.3 g, 10.51 mmol, 1.00 equiv) in tetrahydrofuran (50 mL). n-BuLi (4.4 mL) was added dropwise with stirring at -78 C. The resulting solution was stirred for 10 mins at -78 C. and then tris(propan-2-yl)borate (2.1 g, 11.17 mmol, 1.06 equiv) was added dropwise with stirring at -78 C. over 10 min. The resulting solution was stirred while the temperature warmed from -78 C. to room temperature. The reaction was then quenched by the addition of saturated aqueous NH4Cl and concentrated under vacuum. The resulting solution was diluted with 10% aquious potassium hydroxide and then washed with ether. The pH of the aqueous was adjusted to 2-4 with hydrogen chloride (37%). The resulting solution was extracted with ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum to give 2.2 g (90%) of [4-(2-fluorophenoxy)phenyl]boronic acid as a white solid
  • 2
  • [ 851199-57-0 ]
  • [ 1402238-32-7 ]
YieldReaction ConditionsOperation in experiment
90% Step 4. Into a 100 mL 3-necked round-bottom flask purged and maintained under an inert atmosphere of nitrogen, was placed a solution of 1-(2-fluorophenoxy)-4-iodobenzene (3.3 g,10.51 mmol, 1.00 equiv) in tetrahydrofuran (50 mL). n-BuLi (4.4 mL) was added dropwise with stirring at -78 C. The resulting solution was stirred for 10 mins at -78 C and then tris(propan-2-yl)borate (2.1 g, 11.17 mmol, 1.06 equiv) was added dropwise with stirring at78 C over 10 mm. The resulting solution was stirred while the temperature warmed from -78C to room temperature. The reaction was then quenched by the addition of saturated aqueous NH4Cl and concentrated under vacuum. The resulting solution was diluted with 10% aqueous potassium hydroxide and then washed with ether. The pH of the aqueous was adjusted to 2-4 with hydrogen chloride (37% ). The resulting solution was extracted with ethyl acetate andthe organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum to give 2.2 g (90%) of [4-(2-fluorophenoxy)phenyl]boronic acid as a white solid.
 

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