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Chemical Structure| 151038-76-5 Chemical Structure| 151038-76-5

Structure of 151038-76-5

Chemical Structure| 151038-76-5

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Product Details of [ 151038-76-5 ]

CAS No. :151038-76-5
Formula : C13H10BrClO
M.W : 297.58
SMILES Code : ClC1=CC=C(OCC2=CC=CC=C2)C(Br)=C1
MDL No. :MFCD11870105

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Application In Synthesis of [ 151038-76-5 ]

* 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 [ 151038-76-5 ]

[ 151038-76-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 151038-76-5 ]
  • [ 612832-83-4 ]
YieldReaction ConditionsOperation in experiment
A solution of butyl lithium (1.6 M in hexane) (50 ml) was added drop wise to a stirredsolution of the product from step a) (23 g) in diethylether (300 ml) at -70 C. After 1 h afurther 18 ml of butyl lithium was added, left for 0.75 h, then trimethylborate (10 ml) addedand the mixture warmed to RT and left for 16 h. 2 M Hydrochloric acid (100 ml) was added,stirred for Ih then the organic layer separated and extracted with aqueous sodium hydroxidesolution. The basic layer was acidified with 2 M hydrochloric acid solution, extracted withdiethylether which was dried and evaporated under reduced pressure. The residue wastriturated with iso-hexane and filtered to give the sub-title compound (10.8 g)JH NMR CDC13: 8 7.82 (IH, d); 7.44-7.34 (6H, m) ; 6.90 (IH, d) ; 5.99 (2H, s) ; 5.12 (2H, s)
A solution of butyl lithium (1.6M in hexane) (50ML) was added dropwise to a stirred solution of the product from step (i) (23g) in diethylether (300ml) AT-70C. After lh a further 18ML of butyl lithium was added, left for 0.75h, then trimethylborate (10ML) added and the mixture warmed to RT and left for 16h. 2M Hydrochloric acid (100ml) was added, stirred for lh then the organic layer separated and extracted with aqueous sodium hydroxide solution. The basic layer was acidified with 2M hydrochloric acid solution, extracted with diethylether which was dried and evaporated under reduced pressure. The residue was triturated with iso-hexane and filtered. Yield 10.8g 1H NMR CDC13 : 5 7. 82 (1H, d); 7.44-7. 34 (6H, m); 6.90 (1H, d); 5.99 (2H, s); 5.12 (2H, S)
 

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