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Chemical Structure| 3360-45-0 Chemical Structure| 3360-45-0

Structure of 3360-45-0

Chemical Structure| 3360-45-0

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Product Details of [ 3360-45-0 ]

CAS No. :3360-45-0
Formula : C7H5BrClNO2
M.W : 250.48
SMILES Code : O=[N+](C1=CC(CBr)=CC=C1Cl)[O-]
MDL No. :MFCD12025138

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Application In Synthesis of [ 3360-45-0 ]

* 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 [ 3360-45-0 ]

[ 3360-45-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 22513-32-2 ]
  • [ 3360-45-0 ]
  • [ 4394-33-6 ]
  • 2
  • [ 55912-20-4 ]
  • [ 3360-45-0 ]
YieldReaction ConditionsOperation in experiment
With phosphorus tribromide; In toluene; 4-(bromomethyl)-1-chloro-2-nitrobenzene To a solution of <strong>[55912-20-4](4-chloro-3-nitrophenyl)methanol</strong> (5.0 g, 26.6 mmol) in toluene (100 mL) was added phosphorus tribromide (0.879 mL, 9.32 mmol) at 40 C. The reaction mixture was stirred at 100 C. for 15 mins and partitioned between water and ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound.
With phosphorus tribromide; In dichloromethane; at 0℃; for 1h; Step 1: To a 0C solution of compound 30-1 (0.5 g, 2.67 mmol) in DCM (30 mL) was added PBr3 (0.87 g, 3.20 mmol) drop wise. The reaction was stirred at 0C for 1 nr. then quenched with water (10 m L) and extracted with DCM (30 mL x 3). The combined organic layer was washed with water and brine, dried over Na2S04 and evaporated. The residue was purified by column chromatography (eluent: PE/EA = 10/1) to give 30-2 as a colorless oil. NMR (300 MHz, CDC13) δ 7.90 (s, 1H), 7.60 - 7.51 (m, 2H), 4.47 (s, 2H).
With phosphorus tribromide; In toluene; at 40 - 100℃; for 0.25h; To a solution of <strong>[55912-20-4](4-chloro-3-nitrophenyl)methanol</strong> (5.0 g, 26.6 mmol) in toluene (100 mL) was added phosphorustribromide (0.879 mL, 9.32 mmol) at 40 C. The reaction mixture was stirred at 100 C for 15 mins and partitionedbetween water and ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to givethe title compound.
 

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