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Chemical Structure| 2039-50-1 Chemical Structure| 2039-50-1

Structure of 2039-50-1

Chemical Structure| 2039-50-1

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Product Details of [ 2039-50-1 ]

CAS No. :2039-50-1
Formula : C10H8BrNO
M.W : 238.08
SMILES Code : BrCC1=CC(C2=CC=CC=C2)=NO1
MDL No. :MFCD00159724

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Application In Synthesis of [ 2039-50-1 ]

* 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 [ 2039-50-1 ]

[ 2039-50-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2039-50-1 ]
  • [ 90924-12-2 ]
  • 2
  • [ 90924-12-2 ]
  • [ 2039-50-1 ]
YieldReaction ConditionsOperation in experiment
55.2% With phosphorus tribromide; In diethyl ether; at 20℃; [00230j (3-Phenylisoxazol-5-yl)methanol (2.0 g, 11 mmol) and phosphorus tribromide (1.1 ml, 11 mmol) in ether (30 mL) were stirred overnight at rt. The solution waspartitioned between water/brine and ether. The organic layer was filtered through silica and concentrated to furnish Example 14A (1.5 g, 6.30 mmol, 55.2% yield) as a white solid. 1H NMR (500 MHz, CD3OD) oe 7.83 (dd, J=7.8, 1.8 Hz, 2H), 7.58 - 7.40 (m, 3H), 6.88 (s, 1H), 4.55 (s, 2H).
With phosphorus tribromide; In dichloromethane; at 0℃;Cooling with ice; General procedure: A mixture of b' (10 mmol) in anhydrous CH2Cl2 (25 mL) was cooled to 0 C, a solution of PBr3 (0.95 mL, 10 mmol) in CH2Cl2 (2 mL) was added dropwise and stirred in ice-bath until the raw material consumed. When warmed up to room temperature, the reaction mixture was neutralized with 10% NaOH and extracted with CH2Cl2 two times, The organic phase was evaporated under reduced pressure and purified by silica gel chromatography with petroleum ether/ethyl acetate to give c'.
With phosphorus tribromide; In dichloromethane; at 0℃; General procedure: A mixture of 3 (10 mmol) in anhydrous CH2Cl2 (25 mL) was cooled to 0C, a solution of PBr3 (0.95 mL, 10 mmol) in CH2Cl2 (2 mL) was added dropwise and stirred in ice-bath until the raw material consumed. When warmed up to room temperature, the reaction mixture was neutralized with 10% NaOH and extracted with CH2Cl2 two times, The organic phase was evaporated under reduced pressure and purified by silica gel chromatography with petroleum ether/ethyl acetate to give 4.
 

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