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Chemical Structure| 128092-72-8 Chemical Structure| 128092-72-8

Structure of 128092-72-8

Chemical Structure| 128092-72-8

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Product Details of [ 128092-72-8 ]

CAS No. :128092-72-8
Formula : C19H14F2O
M.W : 296.31
SMILES Code : OC(C1=CC=C(F)C=C1)(C2=CC=CC=C2F)C3=CC=CC=C3
MDL No. :MFCD25977181
Boiling Point : No data available
InChI Key :OBUSEBRACGMKSM-UHFFFAOYSA-N
Pubchem ID :14579819

Safety of [ 128092-72-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 128092-72-8 ]

* 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 [ 128092-72-8 ]

[ 128092-72-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 342-25-6 ]
  • [ 100-58-3 ]
  • [ 128092-72-8 ]
YieldReaction ConditionsOperation in experiment
In tert-butylmethyl ether; 1.2a Synthesis of (2-fluorophenyl)-(4-fluorophenyl)phenylmethanol Phenylmagnesium bromide (1.83 mL, 5.5 mmol) was added dropwise to a tirring solution of <strong>[342-25-6]2,4'-difluorobenzophenone</strong> (1.09 g, 5.0 mmol) in t-butylmethyl ether (12 mL) at room temperature ("rt,"~25° C.). After the addition was complete the reaction was heated at reflux for 3 h. The solution was cooled to rt and was poured in to ice cold 1.0 M HCl (aq) (20 mL). The organics were extracted with EtOAc (3*10 mL) and dried (Na2SO4). Concentration under reduced pressure gave the desired product (2-fluorophenyl)-(4-fluorophenyl)phenylmethanol as a pale brown oil which was used in the next reaction without any further purification.
In tert-butyl methyl ether; at 25℃; for 3h;Heating / reflux; Phenylmagnesium bromide (1.83 mL, 5.5 mmol) was added dropwise to a stirring solution of <strong>[342-25-6]2,4'-difluorobenzophenone</strong> (1.09 g, 5.0 mmol) in t-butylmethyl ether (12 mL) at room temperature ("rt," about 25 0C). After the addition was complete the reaction was heated at reflux for 3 h. The solution was cooled to rt and was poured in to ice cold 1.0 M HCl (aq) (20 mL). The organics were extracted with EtOAc (3 X 10 mL) and dried (Na2SO4). Concentration under reduced pressure gave the desired product (2-fiuorophenyl)- (4-fiuorophenyl)phenylmethanol as a pale brown oil which was used in the next reaction without any further purification.
  • 2
  • [ 342-25-6 ]
  • phenylmagnesium bromide [ No CAS ]
  • [ 128092-72-8 ]
 

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