Preparation method of phosphine ligand and method for phosphine ligand to catalyze and synthetize biaryl and derivatives thereof

A technology for phosphine ligands and biarenes, which is applied to the preparation method of phosphine ligands and the field of catalyzing synthesis of biarenes and derivatives thereof, can solve the problems of high price, difficulty in synthesizing products, difficulty in recovering catalysts, etc. The effect of reducing activity

Active Publication Date: 2009-06-03
上海立科化学科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Commonly used synthetic methods for biaryls include the reaction of aryl diazonium salts with aromatics under the catalysis of copper (I) to generate biaryls. When there are electron-withdrawing groups on each benzene ring, it is difficult to synthesize the desired product by this method.
[0004] Another method is to use Suzuki coupling reaction, that is, aryl boronic acid or its ester is coupled with halogenated aromatic hydrocarbon under the catalysis of transition metal to ge...

Method used

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  • Preparation method of phosphine ligand and method for phosphine ligand to catalyze and synthetize biaryl and derivatives thereof
  • Preparation method of phosphine ligand and method for phosphine ligand to catalyze and synthetize biaryl and derivatives thereof
  • Preparation method of phosphine ligand and method for phosphine ligand to catalyze and synthetize biaryl and derivatives thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0027] Preparation of phosphine ligand 1-(2-diphenylphosphino)phenethyl alcohol:

[0028] Under the protection of nitrogen, add 7.6g of 2-diphenylphosphinobenzaldehyde and 100ml of tetrahydrofuran into a 250ml four-necked flask, and add 50ml of anhydrous ether solution of 1M iodomethane Grignard reagent dropwise under stirring at 20°C. After the addition is complete, heat to reflux React for 90 minutes, cool the reaction to room temperature, pour it into cold saturated ammonium chloride aqueous solution, extract the aqueous phase with ether, combine the organic phases, dry with anhydrous sodium sulfate, concentrate, and separate by silica gel column chromatography to obtain the product, NMR The data are consistent with the literature.

[0029] The reaction formula is:

[0030]

[0031] Application of phosphine ligand 1-(2-diphenylphosphino)phenylethanol: preparation of 4-methylbiphenyl

[0032] Under nitrogen protection, in a 50ml Schlenk bottle, add 111mg 4-fluorotoluene...

Embodiment 2

[0036] Preparation of phosphine ligand (2-diphenylphosphinophenyl) benzyl alcohol:

[0037] Under the protection of nitrogen, add 7.6g of 2-diphenylphosphinobenzaldehyde and 100ml of tetrahydrofuran to a 250ml four-necked flask, and add 50ml of bromophenyl Grignard reagent in tetrahydrofuran (1M) dropwise under stirring at 20°C. After the addition is complete, heat to Reflux for 90 minutes, cool the reaction to room temperature, pour into cold saturated ammonium chloride aqueous solution, extract the aqueous phase with ether, combine the organic phases, dry with anhydrous sodium sulfate, concentrate, and separate by silica gel column chromatography to obtain the product.

[0038] The reaction formula is:

[0039]

[0040] Application of phosphine ligand (2-diphenylphosphinophenyl) benzyl alcohol: preparation of 4-phenylpyridine

[0041] Method A: Add 18g p-4-bromopyridine, 2.355g (2-diphenylphosphinophenyl) benzyl alcohol, 0.82g Ni(acac) to a 500ml four-necked flask under ...

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Abstract

The invention relates to a preparation method of phosphine ligand and a method for the phosphine ligand to catalyze and synthetize biaryl and derivatives thereof. The preparation method of the phosphine ligand comprises the following steps: 2-diphenyl phosphono benzaldehyde is used to react with a Grignard reagent, and the phosphine ligand is acquired; X in the Grignard reagent is halogen, and R is C1-C8 alkyl, aryl or substituted aryl; wherein, the substituted aryl is that one or multiple positions in number 2 to 6 positions of aromatic ring are substituted; and substituent is one or varieties in fluorine, chlorine, phenyl, C1-C8 alkyl and C1-C8 alkoxy. The invention discloses the method of using the phosphine ligand to jointly catalyze and synthetize the biaryl and the derivatives thereof with a nickel catalyst. The invention uses high catalytic activity of the phosphine ligand, TON is usually higher than 2500, and the phosphine ligand is easy to be prepared and suitable for industrial production. The phosphine ligand can be produced by the Grignard reagent and 2-diphenyl phosphono-containing benzaldehyde in the field without separation, and directly catalyze a coupling reaction; and furthermore, the reactivity of the phosphine ligand is not obviously reduced.

Description

technical field [0001] The present invention relates to a method for preparing a phosphine ligand and a method for catalytically synthesizing biaryls and derivatives thereof, in particular to a method for preparing a class of phosphine ligands, and using the phosphine ligands and a nickel catalyst to jointly catalyze the synthesis of biaryls and biaryls. method of its derivatives. Background technique [0002] Biaryl compounds are a class of functional and versatile compounds, often used in liquid crystal materials and pharmaceutical intermediates. For example: 3, 4, 3", 4"-tetramethyl terphenyl is used in conductive polymer materials, and 4'-methyl biphenyl-2-carbonitrile is an intermediate of sartan drugs. [0003] Commonly used synthetic methods for biaryls include the reaction of aryl diazonium salts with aromatics under the catalysis of copper (I) to generate biaryls. When there are electron-withdrawing groups on each benzene ring, it is difficult to synthesize the de...

Claims

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Application Information

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IPC IPC(8): C07F9/50B01J31/24B01J31/04C07D213/06
Inventor 曾志宏高红云许庆贤张芳江
Owner 上海立科化学科技有限公司
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