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[ CAS No. 1378683-82-9 ]

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Chemical Structure| 1378683-82-9
Chemical Structure| 1378683-82-9
Structure of 1378683-82-9 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1378683-82-9 ]

CAS No. :1378683-82-9 MDL No. :MFCD16618125
Formula : C8H5F3O Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W :174.12 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1378683-82-9 ]

* 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 [ 1378683-82-9 ]

[ 1378683-82-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 124004-75-7 ]
  • [ 1378683-82-9 ]
YieldReaction ConditionsOperation in experiment
94.8% Stage #1: α,α,α-trifluoro-2-fluoroacetophenone With chloro-trimethyl-silane; magnesium In tetrahydrofuran at 0 - 20℃; Inert atmosphere; Stage #2: With hydrogenchloride; water at 20℃; for 0.383333h; Cooling with ice; 2,2-difluoro-l-(2-fluoro-phenyl)-ethanone The 2,2-difluoro-l-(2-fluoro-phenyl)-ethanone was obtained as follows: In a dry flask a suspension of magnesium (1.26 g, 52.0 mmol) in THF (100 ml) was treated at r.t. under an inert atmosphere with chloro-trimethyl silane (11.3 g, 13.3 ml, 104 mmol). The suspension was cooled to 0 °C and 2,2,2-trifluoro-l-(2-fluorophenyl)ethanone (4.99 g, 26 mmol) was added dropwise within 4 min while the internal temperature rose to 13 °C. After complete addition the internal temperature has reached 20 °C. Thereafter the suspension was cooled to 0 °C and stirred for 1 hour. For the workup, the yellow solution was allowed to warm to r.t., decanted and hydrochloric acid (37%>; 20.5 g, 17.1 ml, 208 mmol) was added dropwise within 3 minutes while cooling with an ice bath. The turbid solution was stirred at r.t. for 20 min. The mixture was treated with brine (200 ml), and the aqueous layer was separated and extracted twice with AcOEt. The organic layers were washed with a saturated solution of NaHCOs and brine, then dried and evaporated to give after standing at r.t. the 2,2-difluoro-l-(2- fluorophenyl)ethanone (4.292 g, 94.8 % yield) as a light yellow semisolid. MS: m/z = 174 [M]+.
  • 2
  • [ 198967-24-7 ]
  • [ 65864-64-4 ]
  • [ 1378683-82-9 ]
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