Synthesis method of ortho-benzyl diphosphine compound
A synthesis method and technology of phosphine compounds, applied in chemical instruments and methods, organic compound/hydride/coordination complex catalysts, compounds of Group 5/15 elements of the periodic table, etc., can solve low yield and unfavorable industrialization Production and other issues, to achieve high yield, improve safety and controllability, mild and controllable reaction conditions
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[0060] One embodiment of the present invention provides a method for synthesizing an ortho-benzyl bisphosphine compound, comprising the following steps:
[0061] In an organic solvent, α,α'-dihalogenated o-xylene and dihydrocarbyl phosphine are subjected to a substitution reaction under the action of a metal salt catalyst, a ligand and a basic compound to obtain an ortho-benzyl bisphosphine compound.
[0062] Wherein, the metal in the metal salt catalyst is a transition metal, and the ligand can coordinate with the metal salt catalyst.
[0063] Dihydrocarbylphosphine is , R is independently selected from: alkyl, aryl or cycloalkyl.
[0064] In some embodiments, metal salt catalysts and ligands can also be added in a pre-coordinated form.
[0065] The structural formula of α,α'-dihalogenated o-xylene is as follows:
[0066]
[0067] Wherein, X is a halogen, further X is independently selected from Cl or Br.
[0068] The reaction formula of this synthetic method is as fo...
Embodiment 1
[0088] This example is a synthesis method of ortho-benzyl bisphosphine compounds, specifically the synthesis steps of bis(diamantylphosphine)-o-xylene. The whole process is carried out in an anhydrous and oxygen-free environment, and the steps are as follows:
[0089] Under Ar atmosphere, add o-dibromobenzyl (300g, 1eq) to 2L toluene solution to dissolve it completely, then add diadamantyl phosphine hydrogen (687g, 2eq), add metal salt catalyst Pd(OAc) 2 (7.6g, 3%eq), ligand DIPPF (15.7g, 3.3%eq) and tBuONa (279g, 2.5eq), heated to reflux, the solid gradually dissolved, reacted for 4h, TLC monitored the reaction was complete, stopped the reaction and cooled to room temperature .
[0090] Remove the solvent by distillation under reduced pressure, then add dichloromethane to dissolve the solid completely (1L), wash with water (1L×3 times), wash with saturated sodium chloride solution (1L×3 times), dry over anhydrous sodium sulfate, filter, and normal pressure The solvent was di...
Embodiment 2
[0092] This embodiment is a synthesis method of ortho-benzyl bisphosphine compounds, specifically the synthesis steps of bis(diphenylphosphine)-o-xylene. The whole process is carried out in an anhydrous and oxygen-free environment, and the steps are as follows:
[0093] Under Ar atmosphere, add o-dibromobenzyl (300g, 1eq) to 2L toluene solution to dissolve it completely, then add diphenylphosphine hydrogen (423g, 2eq), add metal salt catalyst Pd(OAc) 2 (7.6g, 3%eq), ligand DIPPF (15.7g, 3.3%eq) and tBuONa (279g, 2.5eq), heated to reflux, the solid gradually dissolved, reacted for 4h, TLC monitored the reaction was complete, stopped the reaction and cooled to room temperature .
[0094] Remove the solvent by distillation under reduced pressure, then add dichloromethane to dissolve the solid completely (1L), wash with water (1L×3 times), wash with saturated sodium chloride solution (1L×3 times), dry over anhydrous sodium sulfate, filter, and normal pressure The solvent was dist...
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