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Chemical Structure| 852138-90-0 Chemical Structure| 852138-90-0

Structure of 852138-90-0

Chemical Structure| 852138-90-0

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Product Details of [ 852138-90-0 ]

CAS No. :852138-90-0
Formula : C24H32Br2Si
M.W : 508.40
SMILES Code : CCCCCC[Si]1(CCCCCC)C2=CC(Br)=CC=C2C3=CC=C(Br)C=C31
MDL No. :MFCD16621120

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Application In Synthesis of [ 852138-90-0 ]

* 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 [ 852138-90-0 ]

[ 852138-90-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 852138-89-7 ]
  • [ 18204-93-8 ]
  • [ 852138-90-0 ]
YieldReaction ConditionsOperation in experiment
53% t-BuLi (15.3 mL, 0.0261 mol, 1.7 M in pentane) was slowly added to a solution of 4,4?- dibromo-2,2?-diiodobiphenyl (compound 1, 3.50 g, 6.21 mmol) in dry THF (40 mL), over 30 mins, at 95 O (hexanes/liquid nitrogen) under a nitrogen inert atmosphere. The reaction mixture was stirred for a further one hour at 95 c and dichlorodihexylsilane (3.34 g, 0.0124mol) was subsequently added and was stirred at room temperature overnight. Water (50 mL) was added and the product was extracted into diethylether (3 x 50 mL), the ethereal extracts washed with water (150 mL), dried (Mg504), filtered and concentrated under reduced pressure. The crude product was purified by gravity column chromatography (wet loaded, silica gel, hexanes) to yield compound 2 as a colourless oil (1.67 g, 53%).1H NMR (400 MHz, CDCI3): O (ppm) 0.84 (6 H, t, J = 6.8 Hz, OH3), 0.91-0.95 (4 H, m, OH2),1.18-1.33 (16 H, m, OH2), 7.53 (2 H, dd, J = 2.0 and 8.0 Hz, Ar-H), 7.63 (2 H, d, J = 8.4 Hz, Ar-H), 7.68 (2 H, d, J = 2.0 Hz, Ar-H).
Under the protection of argon, 6.00 g of 4,4?-dibromo-2,2?-diiodo biphenyl was dissolved in 100 mL of THF, cooled to -100 C., then to the solution 42.55 mL of methyl lithium solution (methyl lithium/n-hexane in 1.0 M) was added dropwise. After 12 hours of reaction, 5.70 g dihexyl dichlorosilane was added, and the reaction was continued for another 48 hours, the reaction was completed, then a water was added, and the mixture was extracted with diethyl ether, dried over anhydrous magnesium sulfate, rotary evaporated, and column chromatographed to give the product, MALDI-TOF-MS (m/z): 508.4 (M+);
Under the protection of argon, 6.00 g of 4, 4'-dibromo-2, 2'-diiodo biphenyl was dissolved in 100 mL of THF, cooled to -100 C, then to the solution 42.55 mL of methyl lithium solution (methyl lithium/n-hexane in 1.0 M) was added dropwise. After 12 hours of reaction, 5.70 g dihexyl dichlorosilane was added, and the reaction was continued for another 48 hours, the reaction was completed, then a water was added, and the mixture was extracted with diethyl ether, dried over anhydrous magnesium sulfate, rotary evaporated, and column chromatographed to give the product, MALDI-TOF-MS (m/z): 508.4 (M +);
 

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