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Chemical Structure| 1255208-31-1 Chemical Structure| 1255208-31-1

Structure of 1255208-31-1

Chemical Structure| 1255208-31-1

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Product Details of [ 1255208-31-1 ]

CAS No. :1255208-31-1
Formula : C8H4BrFO2
M.W : 231.02
SMILES Code : O=C1OCC2=C1C=CC(Br)=C2F
MDL No. :MFCD27977405

Safety of [ 1255208-31-1 ]

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 [ 1255208-31-1 ]

* 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 [ 1255208-31-1 ]

[ 1255208-31-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 180307-56-6 ]
  • [ 1255208-31-1 ]
  • [ 1428478-86-7 ]
YieldReaction ConditionsOperation in experiment
With palladium diacetate; triethylamine; In N,N-dimethyl-formamide; at 130℃; for 2.0h; Step B: tert-Butyl 4-[(E)-2-(4-Fluoro-l-oxo-13-dihydro-2-benzofuran-5-yl)ethenyllpiperidine- 1-carboxylate To a flask added 5-bromo-4-fluoro-2-benzofuran-l (3H)-one (0.10 g, 0.43 mmol) palladium(II)acetate (0.097 g, 0.043 mmol), triethylamine (0.12 mL, 0.88 mmol) and tert-butyl 4-ethyenylpiperidine-l-carboxylate (0.27 g, 1.2 mmol); the resulting mixture was then dissolved in DMF (15 mL) and heated in an oil bath at 130 C for 2 h. The flask was cooled to room temperature, diluted with EtOAc and washed with saturated sodium bicarbonate and water, then dried (Na2SC>4), filtered and adsorbed into silica gel. MPLC (hexanes/EtOAc = 1/1) purification provided tert-butyl 4-[(E)-2-(4-fluoro- 1 -oxo- 1 ,3-dihydro-2-benzofuran-5-yl)ethenyl]piperidine- 1-carboxylate. LC/MS: [(M+2)]+ =233.
With palladium diacetate; triethylamine; In N,N-dimethyl-formamide; at 130℃; for 2.0h; [0171] To a flask added 5-bromo-4-fluoro-2-benzofuran-1(3H)-one (0.10 g, 0.43 mmol) palladium(II)acetate (0.097 g,0.043 mmol), triethylamine (0.12 mL, 0.88 mmol) and tent-butyl 4-ethyenylpiperidine-1-carboxylate (0.27 g, 1.2 mmol);the resulting mixture was then dissolved in DMF (15 mL) and heated in an oil bath at 130 C for 2 h. The flask was cooledto room temperature, diluted with EtOAc and washed with saturated sodium bicarbonate and water, then dried (Na2SO4),filtered and adsorbed into silica gel. MPLC (hexanes/EtOAc = 1/1) purification provided tert-butyl 4-[(E)-2-(4-fluoro-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethenyl]piperidine-1-carboxylate. LC/MS: [(M+2)]+ =233.
  • 2
  • [ 180307-56-6 ]
  • [ 1255208-31-1 ]
  • [ 1428478-87-8 ]
 

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