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Chemical Structure| 891182-24-4 Chemical Structure| 891182-24-4

Structure of 891182-24-4

Chemical Structure| 891182-24-4

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Product Details of [ 891182-24-4 ]

CAS No. :891182-24-4
Formula : C28H40Br2Si
M.W : 564.51
SMILES Code : CCCCCCCC[Si]1(CCCCCCCC)C2=CC(Br)=CC=C2C3=CC=C(Br)C=C31
MDL No. :MFCD16619361
InChI Key :FPSGCUROGVMFJQ-UHFFFAOYSA-N
Pubchem ID :57892317

Safety of [ 891182-24-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of [ 891182-24-4 ]

* 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 [ 891182-24-4 ]

[ 891182-24-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 852138-89-7 ]
  • [ 18416-07-4 ]
  • [ 891182-24-4 ]
YieldReaction ConditionsOperation in experiment
40% 4,4'-Dibromo-2,2'-diiodobiphenyl (2.8 g, 4.9 mmol) was dissolved in 90 mL of anhydrous tetrahydrofuran, and a solution of 2.5 M n-butyllithium in n-hexane was added at -78 C.(7.8mL, 19.5mmol), heat preservation reaction for 1 hour,Dioctyldichlorosilane (1.8 g, 5.4 mmol) was then added rapidly.The reaction was incubated for 30 minutes, after which the reaction solution was allowed to warm to room temperature overnight.After the reaction is completed, the reaction is quenched with water, extracted, and the organic phase is washed with brine.Dry and purify by column chromatography to give a white solid (1,1g, 40%)
In 85 ml of tetrahydrofuran (produced by Wako Pure Chemical Industries, Ltd.) was dissolved 4.27 g of the compound (10-d), and the resulting solution was cooled to -80C. After adding 19 ml of a 1.6 M hexane solution of n-butyl lithium (produced by Wako Pure Chemical Industries, Ltd.) over 1 hour, the resulting mixture was stirred under a nitrogen atmosphere at -80C for 30 minutes. 5.2 ml of dichlorodioctylsilane (produced by Wako Pure Chemical Industries, Ltd.) was added, and the temperature of the resulting mixture was raised to room temperature and the mixture was stirred under a nitrogen atmosphere for one day. To the resulting solution was added 50 ml of water and the solvent was distilled off. After adding 150 ml of diethyl ether, an organic layer was fractionated, washed with 400 ml of water, and then dried with magnesium sulfate. The resulting solution was purified by column chromatography (filler: silica gel, eluent: hexane) to obtain 2.49 g of compound (10-e).
 

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