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Chemical Structure| 680610-73-5 Chemical Structure| 680610-73-5

Structure of 680610-73-5

Chemical Structure| 680610-73-5

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Product Details of [ 680610-73-5 ]

CAS No. :680610-73-5
Formula : C9H9BrFNO2
M.W : 262.08
SMILES Code : O=C(N(OC)C)C1=CC=CC(Br)=C1F
MDL No. :MFCD21609714

Safety of [ 680610-73-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 680610-73-5 ]

* 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.

  • Upstream synthesis route of [ 680610-73-5 ]
  • Downstream synthetic route of [ 680610-73-5 ]

[ 680610-73-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 680610-73-5 ]
  • [ 75-16-1 ]
  • [ 161957-61-5 ]
YieldReaction ConditionsOperation in experiment
97%
Stage #1: at -78 - 20℃;
Stage #2: With hydrogenchloride In tetrahydrofuran; diethyl ether; water at 0℃;
1-(3-Bromo-2-fluorophenyl)-ethanone [161957-61-5]
Methylmagnesium bromide (3 M in diethyl ether, 21 mL) was added to 3-bromo-2-fluoro-N-methoxy-N-methylbenzamide (10.89 g) in tetrahydrofuran (100 mL) at -78° C.
This was allowed to warm to room temperature and stir for 16 h.
The reaction was then cooled to 0° C. and carefully quenched with 2 M HCl until pH=1.
The solvent was removed by evaporation and the product extracted with ethyl acetate (3*100 mL).
The organic layers were combined, dried over sodium sulfate and the solvent removed by evaporation to yield the product as a light brown solid.
This was dissolved in dichloromethane (200 mL) and washed with sat. NaHCO3 (200mL).
The dichloromethane layer was dried over sodium sulfate and the solvent removed by evaporation to yield 1-(3-bromo-2-fluorophenyl)-ethanone as a yellow oil (8.8 g, 97percent).
1H NMR (CDCl3): 2.67 (3H, d, ArCOCH3), 7.11 (1H, t, Ar), 7.69-7.81 (2H, m, Ar).
64% at 0℃; for 2 h; Methylmagnesium bromide (0.8 mL of a 1.4 M solution in THF/toluene), was added to a solution of 3-Bromo-2-fluoro-N-methoxy-N-methyl-benzamide (190 g, 0.73 mmol) in THF (1 mL) at 0° C. and the reaction was stirred at 0° C. for 2 h. The reaction was quenched with dilute aqueous HCl and extracted with EtOAc. The organics were dried over MgSO4, concentrated and chromatographed to provide 100 mg (64percent yield) of the title compound as colorless oil.
References: [1] Patent: US2009/209529, 2009, A1, . Location in patent: Page/Page column 34.
[2] Patent: US2008/76771, 2008, A1, . Location in patent: Page/Page column 18.
 

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