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Chemical Structure| 870061-72-6 Chemical Structure| 870061-72-6

Structure of 870061-72-6

Chemical Structure| 870061-72-6

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Product Details of [ 870061-72-6 ]

CAS No. :870061-72-6
Formula : C9H9BrO
M.W : 213.07
SMILES Code : BrCC1=C(OCC2)C2=CC=C1
MDL No. :MFCD16037372

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Application In Synthesis of [ 870061-72-6 ]

* 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 [ 870061-72-6 ]

[ 870061-72-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 151155-53-2 ]
  • [ 870061-72-6 ]
YieldReaction ConditionsOperation in experiment
With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 0 - 20℃; EXAMPLE 29B 7-(bromomethyl)-2,3-dihydro-1-benzofuran Example 29A (4.06 g, 27.1 mmol) and carbon tetrabromide (10.9 g, 32.8 mmol) were combined in methylene chloride (100 mL) at 0 C. and treated with triphenylphosphine (8.53 g, 32.6 mmol) portionwise. The mixture was allowed to warm to room temperature, was stirred overnight, concentrated under reduced pressure, and the residue was purified by flash chromatography (2% ethyl acetate/hexanes) to provide the title compound. 1H NMR (CDCl3) δ 3.22 (t, 2H), 4.50 (s, 2H), 4.65 (t, 2H), 6.81 (t, 1H), 7.12 (m, 2H).
With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 0 - 20℃; The product of Example 48A (4.06 g) and carbon tetrabromide (10.9 g) were combined in methylene chloride (100 mL) at 0 C and treated with triphenylphosphine (8.53 g) portionwise. The mixture was allowed to warm to room temperature, stirred overnight, concentrated under reduced pressure, and the residue was purified by flash chromatography (2% ethyl acetate/hexanes) to provide the title compound. 1H NMR (CDC13) 3.22 (t, 2H), 4.50 (s, 2H), 4.65 (t, 2H), 6.81 (t, 1H), 7.12 (m, 2H).
 

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