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Chemical Structure| 53244-91-0 Chemical Structure| 53244-91-0

Structure of 53244-91-0

Chemical Structure| 53244-91-0

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Product Details of [ 53244-91-0 ]

CAS No. :53244-91-0
Formula : C8H5BrCl2O2
M.W : 283.93
SMILES Code : OC1=C(Cl)C=C(Cl)C=C1C(CBr)=O

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Application In Synthesis of [ 53244-91-0 ]

* 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 [ 53244-91-0 ]

[ 53244-91-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3321-92-4 ]
  • [ 53244-91-0 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; trimethylsilyl trifluoromethanesulfonate; In acetonitrile; at 40℃;Darkness; General procedure: Ketone (1 eq) and N-bromosuccinimide (NBS) (2 eq) were solved in acetonitrile and trimethylsilyl trifluoromethanesulfonate (TMS-OTf) (1 eq) was added. The reactions were stirred at T = 40 C until completeness, diluted with diethyl ether (2 ml), washed with H2O (3 x 2 ml), dried over Na2SO4 and concentrated under reduced pressure. This procedure provided bromoketones intermediates in 75-90% overall yield, with purities generally >90% as determined by HPLC-MS. The compounds was used without further purification.
With copper(ll) bromide; In ethyl acetate; for 10h;Reflux; General procedure: CuBr2 (450 mg, 2.0 mmol) was added to a solution of commercially available, substituted o-hydroxyacetophenone (1.0 mmol) in EtOAc (30 mL) at 25 C. The reaction mixture was stirred at reflux for 10 h. Then, the reaction mixture was cooled to 25 C, filtered, neutralized with saturated aq NaHCO3 (30 mL) and extracted with EtOAc (3 × 30 mL). The combined organic layers were washed with brine, dried, filtered and evaporated under reduced pressure to afford crude product. Without further purification, substituted sodium sulfinate (2.1 mmol) was added to the resulting substituted α-bromo-o-hydroxyacetophenone in a cosolvent of dioxane and water [20 mL, 1:1 (v/v)] at 25 C. The reaction mixture was stirred at reflux for 3 h. Then, the reaction mixture was cooled to 25 C and extracted with CH2Cl2 (3 × 30 mL). The combined organic layers were washed with brine, dried, filtered and evaporated under reduced pressure to afford crude product. Purification on silica gel (hexanes/EtOAc, 10:1-2:1) afforded skeleton 1, known compounds whose analytical data are consistent with the literature.12b
 

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