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Chemical Structure| 63574-45-8 Chemical Structure| 63574-45-8

Structure of 63574-45-8

Chemical Structure| 63574-45-8

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Product Details of [ 63574-45-8 ]

CAS No. :63574-45-8
Formula : C8H8BrNO2
M.W : 230.06
SMILES Code : BrC1=C2OCCOC2=C(N)C=C1
MDL No. :MFCD29938201

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Application In Synthesis of [ 63574-45-8 ]

* 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 [ 63574-45-8 ]

[ 63574-45-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 16081-45-1 ]
  • [ 63574-45-8 ]
YieldReaction ConditionsOperation in experiment
77% With N-Bromosuccinimide; In acetonitrile; at 0 - 20℃; for 3h; At 0C, a solution of N-bromosuccinimide (1.73g, 9.73mmol) in acetonitrile (5mL) was added to a solution ofcompound 11-f (1.4g, 9.27mmol) in acetonitrile (35mL). The mixture was warmed to room temperature and reacted for3hrs, evaporated under reduced pressure to remove the solvent. The residue was purified by silica column chromatography(PE:EA = 10:1 to 5:1) to give compound 11-e (1.63g, yield 77%). LC-MS (ESI): m/z = 230 [M+H]+.
30 g With N-Bromosuccinimide; In N,N-dimethyl-formamide; at -30℃; for 1h; dropwise a solution of N-bromosuccinimide (47 g) in DMF (250 mL). The mixture is stirred for 1 hour and is then poured into a water/ice mixture (500 mL/500 g); the precipitate that forms is dissolved in methylene chloride. The organic phase is dried over MgSO4 and then concentrated in vacuo. Intermediate 116a is obtained in the form of a violet solid (30 g). 1H NMR (400 MHz, DMSO-d6): δ 6.78 (d, 1H), 6.20 (d, 1H), 4.25 (m, 4H), 4.90 (s, 2H) IR (cm-1): 3480
  • 2
  • [ 4442-53-9 ]
  • [ 63574-45-8 ]
 

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