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Chemical Structure| 952586-77-5 Chemical Structure| 952586-77-5

Structure of 952586-77-5

Chemical Structure| 952586-77-5

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Product Details of [ 952586-77-5 ]

CAS No. :952586-77-5
Formula : C22H22BrFeP
M.W : 453.13
SMILES Code : Br[C-]12[Fe+2]3456789(C1=C7C8=C29)[C-]%10(P(C%11CCCCC%11)C%12CCCCC%12)C3=C4C5=C6%10
MDL No. :N/A

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Application In Synthesis of [ 952586-77-5 ]

* 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 [ 952586-77-5 ]

[ 952586-77-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1293-65-8 ]
  • [ 16523-54-9 ]
  • [ 952586-77-5 ]
YieldReaction ConditionsOperation in experiment
84% 120 ml (0.3 mol) of n-BuLi (2.5 M in hexane) are added dropwise at a temperature of <-30C to a solution of 103 g (0.3 mol) of 1 ,1 '-<strong>[1293-65-8]dibromoferrocene</strong> in 300 ml of THF. The mixture is stirred further at this temperature for 1.5 hours. The mixture is then cooled to -500C, and 66.2 ml (0.3 mol) of dicyclohexylphosphine chloride are slowly added dropwise at such a rate that the temperature does not rise above -45C. After stirring for a further 10 minutes, the temperature is allowed to rise to room temperature and the mixture is stirred for another one hour. After adding 150 ml of water, the reaction mixture is extracted by shaking with hexane. The organic phases are dried over sodium sulphate, and the solvent is distilled off under reduced pressure on a rotary evaporator. The residue is crystallized in ethanol. The product 13 is obtained with a yield of 84% (yellow solid). 1H NMR (300 MHz, C6D6): delta 1.20-2.11 (m, 22H), 3.97 (m, 2H), 4.23 (m, 2H), 4.26 (m, 2H), 4.41 (m, 2H). 31P NMR (121.5 MHz, C6D6): delta -8.3 (s).
84% To a solution of 103 g (0.3 mol) of 1 ,1 '-<strong>[1293-65-8]dibromoferrocene</strong> in 300 ml of THF are added dropwise, at a temperature of < -300C, 120 ml (0.3 mol) of n-BuLi (2.5 M in hexane). <n="34"/>The mixture is stirred at this temperature for a further 1.5 hour. The mixture is then cooled to -500C, and 66.2 ml (0.3 mol) of dicyclohexylphosphine chloride are added dropwise sufficiently slowly that the temperature does not rise above -45C. After stirring for a further 10 minutes, the temperature is allowed to rise to room temperature and the mixture is stirred for another hour. After 150 ml of water have been added, the reaction mixture is extracted by shaking with hexane. The organic phases are dried over sodium sulphate and the solvent is distilled off under reduced pressure on a rotary evaporator. The residue is crystallized in ethanol. The product A2 is obtained with a yield of 84% (yellow solid).31P NMR (121.5 MHz, C6D6): delta -8.3 (s); 1H NMR (300 MHz, C6D6): delta 4.41 (m, 2H), 4.26 (m, 2H), 4.23 (m, 2H), 3.97 (m, 2H), 1.20-2.11 (m, 22H).
 

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