CN1396194A - Process for preparing biphenyl polyimide - Google Patents
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- CN1396194A CN1396194A CN 02123897 CN02123897A CN1396194A CN 1396194 A CN1396194 A CN 1396194A CN 02123897 CN02123897 CN 02123897 CN 02123897 A CN02123897 A CN 02123897A CN 1396194 A CN1396194 A CN 1396194A
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Abstract
A process for preparing biphenyl polyimide includes such steps as dissolving bichlorodiphthalimide monomer, triphenylphosphino nickel as catalyst and zinc powder as reducer in non-proton solvent, reaction at 60-120 deg.C to generate Ni mating substance, oxydizing addition reaction on bichlorodiphthalimide to generate intermediate, and dereducing reaction to generate its condensate and zinc chloride while reducing Ni to react on chloroimide to generate polyimide. Its advantages are simple process and low cost.
Description
Technical field:
The invention belongs to the preparation method of biphenyl polyimide.
Background technology:
Biphenyl polyimide is as a kind of macromolecular material, because its special performance and application prospects thereof and extremely pay attention to.United States Patent (USP) [Itatani, US Pat., 4 568 715 (1986); Itatani, US Pat., 4 247 443 (1981); Sasaki, US Pat., 4 290 936 (1981); Sasaki, US Pat., 4 473 523 (1984); Kaneda, T., J.Appl.Polym.Sci; 32,3151 (1986) etc.] disclosed traditional biphenyl polyimide preparation method obtains polyimide by biphenyl dianhydride and diamine reactant.Because the synthesis step of biphenyl dianhydride is many, and the catalyzer costliness, or productive rate is lower, or severe reaction conditions, or separates purification difficult, cause the production cost of biphenyl polyimide too high, thereby range of application is restricted.
Summary of the invention:
The preparation method who the purpose of this invention is to provide a kind of biphenyl polyimide.
Feature of the present invention is to synthesize two chloro two phthalimides by chloro-benzoic anhydride that is easy to get and diamine reactant with 2: 1 mol ratio, under the transition-metal catalyst effect, two chloro two phthalimide generation linked reactions are directly synthesized biphenyl polyimide, have saved the step of synthetic biphenyl dianhydride.
The present invention realizes like this, with two chloro two phthalimide monomers, see nickel catalyzator and reductive agent zinc powder of triphenyl is dissolved in the aprotic solvent, in the time of 60～120 ℃, the nickelous title complex reacts under the effect of reductive agent zinc and generates the zero-valent nickel title complex, itself and two chloro two phthalimide monomer generation oxidation addition reactions, generation contains the intermediate of two phenyl nickel, reduction reaction takes place to eliminate then, generate the condenses and the zinc chloride of two chloro two phthalimides, the nickel species are reduced simultaneously, continue and the chloro imide reaction, form catalytic cycle, generate polyimide.The present invention adopts following component to synthesize biphenyl polyimide: two chloro two phthalimides:
The position of substitution of two chlorine atoms can be 4,4`, 3,3` or 3,4.
The diamines of R representative has:
Ursol D, mphenylenediamine, p-diaminodiphenyl; 4, the 4`-diaminodiphenyl oxide; 3,4`-diaminodiphenyl oxide, 4,4`-diamino-ditane, 3,3`-dimethyl-4,4`-diamino-ditane, 4,4`-diamino-diphenyl sulfide, 4,4`-diamino-sulfobenzide, 4, the different propane of 4`-diamino-phenylbenzene, 4,4`-diamino-two phenoxy groups-4``, 4```-biphenyl; 4,4`-diamino-two phenoxy groups-4``, 4```-phenyl ether, 4,4`-diamino-two phenoxy groups-4``, 4```-sulfobenzide, 2,2`-two chloro-4,4`-diamino-ditane, 3,3` two chloro-4,4`-diamino-ditane, 1, the 6-hexanediamine, 4,4`-diamino-phenylbenzene-4``, 4```-benzene diether, 4,4`-diamino-two phenoxy groups-4``, the different propane of 4```-phenylbenzene; 2,2`, 3,3`-tetramethyl--4,4`-diamino-ditane.
Reductive agent is: zinc powder.
Catalyzer is: triphenylphosphine nickelous bromide [(Ph
3)
2NiBr
2] or the triphenylphosphine nickelous chloride
[(Ph
3)
2NiCl
2] nickelous bromide and triphenylphosphine or nickelous chloride and triphenylphosphine.
Aprotic solvent is:
N, dinethylformamide (DMF), N,N-dimethylacetamide (DMAc),
N-N-methyl-2-2-pyrrolidone N-(NMP), dimethyl sulfoxide (DMSO) (DMSO), the tetramethylene sulfone synthesis step is as follows:
With 5～10mmol nickelous bromide or nickelous chloride, 20～80mmol triphenyl is seen and 50～400mmol zinc powder joins in the reaction flask, fill the nitrogen deoxygenation, add 25～40ml aprotic solvent, at 60～120 ℃ of stirring reactions, add two chloro two phthalimides of 115～620ml aprotic solvent and 50-125mmol, reaction 2～8h, then reactant is poured in 1000～1500ml ethanol and the 60～100ml concentrated hydrochloric acid, stir 10～20min, filter, get product, with 300～1000ml alcohol reflux, 2～4h, filter 100～120 ℃ of oven dry, productive rate 95～100%, cresols is a solvent, measures logarithmic viscosity number 0.11～0.98dl/g down for 30 ℃.
The present invention first with two chloro imide in aprotic solvent, be catalyzer with the transiting metal nickel, direct synthetic macromolecule amount biphenyl polyimide.Comparing with prior synthesizing method, saved the synthetic of biphenyl dianhydride, reduced above building-up reactions of 4 steps, is the effective ways that reduce the biphenyl polyimide production cost.
Embodiment is as follows:
Embodiment 1:
With the 5mmol nickelous bromide, 20mmol triphenylphosphine and 50mmol zinc powder join in the reaction flask, fill the nitrogen deoxygenation, add 25ml DMAc, at 120 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 115ml DMAc and 50mmol 4, two (the 4-chloro imide) phenyl ether of 4`-, reaction 2h pours reactant in the 1000ml ethanol then, adds the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 500ml alcohol reflux 2h, filter, 100 ℃ of oven dry get the 22.2g product, productive rate 97%, cresols is a solvent, measures logarithmic viscosity number 0.2dl/g in the time of 30 ℃.
Embodiment 2:
With the 5mmol nickelous bromide, the 80mmol triphenyl is seen and the 200mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 30ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 115ml DMAc and 50mmol 4, two (the 3-chloro imide) phenyl ether of 4`-, reaction 5h pours reactant in the 1000ml ethanol then, adds the 90ml concentrated hydrochloric acid, stir 20min, filter, get product, with 30ml alcohol reflux 2h, filter, 100 ℃ of oven dry get the 22.0g product, productive rate 96%, cresols is a solvent, measures logarithmic viscosity number 0.25dl/g down for 30 ℃.
Embodiment 3:
With the 5mmol nickelous bromide, the 60mmol triphenyl is seen and the 400mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 620ml DMAc and 62.5mmol 4, two (4-chloro imide) two phenoxy groups-4`` of 4`-, 4```-phenyl ether, reaction 3h, reactant is poured in the 1500ml ethanol then, add the 100ml concentrated hydrochloric acid, stir 10min, filter, get product, with 500ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 39.3g product, productive rate 98%, cresols are solvent, 30 ℃ of following logarithmic viscosity number 0.21dl/g.
Embodiment 4:
With the 5mmol nickelous chloride, the 30mmol triphenyl is seen and the 400mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 100 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 350ml DMAc and 50mmol 4, two (the 3-chloro imide) ditanes of 4`-, reaction 3h pours reactant in the 1000ml ethanol then, adds the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 300ml alcohol reflux 2h, filter, 120 ℃ of oven dry get the 22.1g product, productive rate 97%, cresols is a solvent, 30 ℃ of following logarithmic viscosity number 0.2dl/g.
Embodiment 5:
With the 8mmol nickelous bromide, the 80mmol triphenyl is seen and the 300mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 120 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 400ml DMAc and 70mmol 4, two (the 4-chloro imide) biphenyl of 4`-, reaction 2h pours reactant in the 1500ml ethanol then, adds the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 50ml alcohol reflux 4h, filter, 100 ℃ of oven dry get the 29.6g product, productive rate 95%, cresols is a solvent, 30 ℃ of following logarithmic viscosity number 0.11dl/g.
Embodiment 6:
With the 10mmol nickelous bromide, the 80mmol triphenyl is seen and the 250mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 95 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 300ml DMAc and 125mmol 2, the different propane of 2`-(4, two (the 3-chloro imide) phenylbenzene of 4`-), reaction 4h, reactant is poured in the 1500ml ethanol then, add the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 500ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 59g product, productive rate 97%, cresols are solvent, 30 ℃ of following logarithmic viscosity number 0.26dl/g.
Embodiment 7:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 200mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add the 40ml tetramethylene sulfone, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 400ml tetramethylene sulfone and 50mmol 4, two (the 4-chloro imide) sulfobenzides of 4`-, reaction 2h pours reactant in the 1500ml ethanol then, adds the 60ml concentrated hydrochloric acid, stir 20min, filter, get product, with 500ml alcohol reflux 2h, filter, 120 ℃ of oven dry get the 24.7g product, productive rate 97%, cresols is a solvent, 30 ℃ of following logarithmic viscosity number 0.21dl/g.
Embodiment 8:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 60mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 250ml DMAc and 60mmol 4, two (the 3-chloro imide) diphenyl sulfides of 4`-, reaction 3h pours reactant in the 1500ml ethanol then, adds the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 500ml alcohol reflux 3h, filter, 100 ℃ of oven dry get the 27.8g product, productive rate 97%, cresols is a solvent, 30 ℃ of following logarithmic viscosity number 0.2dl/g.
Embodiment 9:
With the 10mmol nickelous bromide, the 70mmol triphenyl is seen and the 400mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 400ml DMAc and 100mmol 4, two (the 3-chloro imide) benzene of 4`-, reaction 7h pours reactant in the 1500ml ethanol then, adds the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 500ml alcohol reflux 2h, filter, 100 ℃ of oven dry get the 36.3g product, productive rate 98%, cresols is a solvent, 30 ℃ of following logarithmic viscosity number 0.17dl/g.
Embodiment 10:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 250mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 400ml DMAc and 50mmol N, phenyl between N--two (4-chloro imide), reaction 5h pours reactant in the 1500ml ethanol then, adds the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 500ml alcohol reflux 2h, filter, 100 ℃ of oven dry get the 18g product, productive rate 97%, logarithmic viscosity number 0.16dl/g (cresols is a solvent, 30 ℃).
Embodiment 11:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 200mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 550ml DMAc and 80mmol 4, two (4-chloro imide) two phenoxy groups-4`` of 4`-, 4```-biphenyl, reaction 4h, reactant is poured in the 1500ml ethanol then, add the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 500ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 48.9g product, productive rate 97%, cresols are solvent, 30 ℃ of following logarithmic viscosity number 0.2dl/g.
Embodiment 12:
With the 5mmol nickelous bromide, the 40mmol triphenyl is seen and the 300mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 400ml DMAc and 50mmol 4, two (4-chloro phthalimide) two phenoxy groups-4`` of 4`-, 4```-sulfobenzide, reaction 7h, reactant is poured in the 1500ml ethanol then, add the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 50ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 33.6g product, productive rate 97%, cresols are solvent, 30 ℃ of following logarithmic viscosity number 0.2dl/g.
Embodiment 13:
With the 5mmol nickelous bromide, the 40mmol triphenyl is seen and the 300mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMSO, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 400mlDMSO and 50mmol 3, two (the 4-chloro imide) phenyl ether of 4-, reaction 7h pours reactant in the 1500ml ethanol then, adds the 60ml concentrated hydrochloric acid, stir 20min, filter, get product, with 500ml alcohol reflux 2h, filter, 100 ℃ of oven dry get the 22.2g product, productive rate 97%, cresols is a solvent, 30 ℃ of following logarithmic viscosity number 0.23dl/g.
Embodiment 14:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 320mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 400ml DMAc and 80mmol 3,3`-dimethyl-two (4-chloro imide)-4,4`-ditane, reaction 8h, then reactant is filtered, get filtrate, then it is sunk in the 1000ml ethanol with the thread shape, get white depositions, filter, with 500ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 38.7g product, productive rate 100%, cresols are solvent, 30 ℃ of following logarithmic viscosity number 0.98dl/g.
Embodiment 15:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 250mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 25ml DMAc, at 95 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 115ml DMAc and 100 pairs of (4-chloro imides)-1, the 6-hexane, reaction 3h sinks in the 1000ml ethanol then, adds the 60ml concentrated hydrochloric acid, get white depositions, stir 10min, filter, with 500ml alcohol reflux 2h, filter, 100 ℃ of oven dry get the 34g product, productive rate 97%, cresols is a solvent, 30 ℃ of following logarithmic viscosity number 0.16dl/g.
Embodiment 16:
With the 5mmol nickelous bromide, the 40mmol triphenyl is seen and the 200mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 95 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 400ml DMAc and 60mmol 4, two (3-chloro the imide)-two phenoxy groups-4`` of 4`-, the different propane of 4```-phenylbenzene, reaction 7h, reactant is poured in the 1500ml ethanol then, add the 60ml concentrated hydrochloric acid, stir 10min, filter, get product, with 500ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 39.7g product, productive rate 99%, cresols are solvent, 30 ℃ of following logarithmic viscosity number 0.36dl/g.
Embodiment 17:
With the 5mmol nickelous bromide, the 40mmol triphenyl is seen and the 100mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml NMP, at 95 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 200ml NMP and 50mmol 3,3`-dimethyl-two (3-chloro imide)-4,4`-ditane, reaction 6h, then reactant is filtered, get filtrate, then it is sunk in the 1000ml ethanol with the thread shape, get white depositions, filter, with 500ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 23.7g product, 98%, 30 ℃ of cresols of productive rate is a solvent, logarithmic viscosity number 0.25dl/g.
Embodiment 18
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 360mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 35ml DMAc, at 95 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 500ml DMAc and 90mmol 2,2`, 3,3`-tetramethyl--two (4-chloro imide)-4,4`-ditane, reaction 7h, then reactant is filtered, get filtrate, then it is sunk in the 1500ml ethanol with the thread shape, get white depositions, filter, with 1000ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 46g product, productive rate 100%, cresols are solvent, 30 ℃ of logarithmic viscosity number 0.77dl/g.
Embodiment 19:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 260mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMF, at 95 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 400ml DMF and 55mmol 2, two (the 4-chloro imides)-4 of 2`-two chloro-, 4`-ditane, reaction 5h, then reactant is filtered, get filtrate, then it is sunk in the 1000ml ethanol with the thread shape, get white depositions, filter, with 500ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 28g product, 98%, 30 ℃ of cresols of productive rate is a solvent, logarithmic viscosity number 0.24dl/g.
Embodiment 20:
With 5mmol (Ph
3)
2NiCl
2, the 50mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, at 60 ℃ of stirring reactions, add 200ml DMAc and 50mmol 3,3`-dimethyl-two (3-chloro imide)-4, the 4`-ditane, reaction 7h filters reactant, pour 1000ml ethanol then into, get product, with 300ml alcohol reflux 2h, filter, 100 ℃ of oven dry get the 23g product, 95%, 30 ℃ of cresols of productive rate is a solvent, logarithmic viscosity number 0.11dl/g.
Embodiment 21:
With 5mmol (Ph
3)
2NiBr
2, the 20mmol triphenyl is seen and the 360mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, adds 40ml DMAc, at 90 ℃ of stirring reactions, add 400mlDMAc and 90mmol 3,3`-dimethyl-two (4-chloro imide)-4, the 4`-ditane, reaction 7h filters reactant then, pour 1500ml ethanol into, get product, with 1000ml alcohol reflux 2h, filter, oven dry gets the 46g product, 100%, 30 ℃ of cresols of productive rate is a solvent, logarithmic viscosity number 0.72dl/g.
Embodiment 22:
With 5mmol (Ph
3)
2NiCl
2, the 20mmol triphenyl is seen and the 360mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, adds 40ml DMAc, at 90 ℃ of stirring reactions, add 400mlDMAc and 90mmol 3,3`-dimethyl-two (4-chloro imide)-4, the 4`-ditane, reaction 7h filters reactant, pour 1500ml ethanol then into, get product, with 1000ml alcohol reflux 2h, filter, 100 ℃ of oven dry get the 46g product, 100%, 30 ℃ of cresols of productive rate is a solvent, logarithmic viscosity number 0.47dl/g.
Embodiment 23:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 150mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 115ml DMAc and 50mmol 3,3`-dimethyl-two (4-chloro imide)-4, the 4`-ditane, reaction 8h filters reactant then, get filtrate, then it is sunk in the 1000ml ethanol with the thread shape, get white depositions, filter, with 500ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 25.5g product, productive rate 100%, cresols is a solvent, 30 ℃ of following logarithmic viscosity number 0.56dl/g.
Embodiment 24:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 400mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 620ml DMAc and 125mmol 3,3`-dimethyl-two (4-chloro imide)-4,4`-ditane, reaction 4h, then reactant is filtered, get filtrate, then it is sunk in the 1500ml ethanol with the thread shape, get white depositions, filter, with 1000ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 64g product, productive rate 100%, cresols are solvent, 30 ℃ of following logarithmic viscosity number 0.56dl/g.
Embodiment 25:
With the 5mmol nickelous bromide, the 20mmol triphenyl is seen and the 50mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 25ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 115ml DMAc and 50mmol 3,3`-dimethyl-two (4-chloro imide)-4,4`-ditane, reaction 2h, then reactant is filtered, get filtrate, then it is sunk in the 1000ml ethanol with the thread shape, get white depositions, filter, with 300ml alcohol reflux 2h, filter 100 ℃ of oven dry, get the 25g product, productive rate 99%, cresols are solvent, 30 ℃ of following logarithmic viscosity number 0.35dl/g.
Embodiment 26:
With the 5mmol nickelous bromide, the 35mmol triphenyl is seen and the 400mmol zinc powder joins in the reaction flask, fills the nitrogen deoxygenation, add 40ml DMAc, at 90 ℃ of stirring reactions, after the system for the treatment of becomes sorrel, add 620ml DMAc and 125mmol 3,3`-dimethyl-3``, 4-dichloro-imide-4`, the 4``-ditane, reaction 4h filters reactant then, gets filtrate, then it is sunk in the 1500ml ethanol with the thread shape, get white depositions, filter, with 1000ml alcohol reflux 2h, filter, 100 ℃ of oven dry get the 64g product, productive rate 100%, cresols is a solvent, 30 ℃ of following logarithmic viscosity number 0.60dl/g.
Claims (3)
1, a kind of preparation method of biphenyl polyimide, its main preparation process is:
With 5～10mmol catalyzer, 20～80mmol triphenyl is seen and 50～400mmol reductive agent joins in the reaction flask, fill the nitrogen deoxygenation, add 25～40ml aprotic solvent, at 60～120 ℃ of stirring reactions, add two chloro two phthalimides of 115～620ml aprotic solvent and 50～125mmol, reaction 2～8h, then reactant is poured in 1000～1500ml ethanol and the 60～100ml concentrated hydrochloric acid, stirred 10～20min, filter, with 300～1000ml alcohol reflux, 2～4h, filter, 100～120 ℃ of oven dry obtain product;
The structure of described pair of chloro two phthalimides as shown in the formula:
The position of substitution of two chlorine atoms can be 4 in the formula, 4` or 3,3` or 3,4;
The diamines of R representative has:
Ursol D, mphenylenediamine, p-diaminodiphenyl, 4, the 4`-diaminodiphenyl oxide, 3, the 4`-diaminodiphenyl oxide, 4,4`-diamino-ditane, 3,3`-dimethyl-4,4`-diamino-ditane, 4,4`-diamino-diphenyl sulfide, 4,4`-diamino-sulfobenzide, 4, the different propane of 4`-diamino-phenylbenzene, 4,4`-diamino-two phenoxy groups-4``, 4```-biphenyl, 4,4`-diamino-two phenoxy groups-4``, the 4```-phenyl ether, 4,4`-diamino-two phenoxy groups-4``, the 4```-sulfobenzide, 3,3` two chloro-4,4`-diamino-ditane, 1, the 6-hexanediamine, 4,4`-diamino-two phenoxy groups-4``, the different propane of 4```-phenylbenzene or 2,2`, 3,3`-tetramethyl--4,4`-diamino-ditane;
Described reductive agent is a zinc powder;
Described catalyzer is the triphenylphosphine nickel halogenide;
Described aprotic polar solvent is N, dinethylformamide, N,N-dimethylacetamide, N-N-methyl-2-2-pyrrolidone N-, dimethyl sulfoxide (DMSO) or tetramethylene sulfone.
2, preparation method as claimed in claim 1 is characterized in that, described catalyzer is nickel halogenide and triphenylphosphine.
3, preparation method as claimed in claim 1 or 2 is characterized in that, described nickel halogenide is nickelous bromide or nickelous chloride.
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1298766C (en) * | 2005-06-20 | 2007-02-07 | 四川大学 | Polyarylene imide sulfide sulfone and its preparation method |
| CN101392055B (en) * | 2007-09-18 | 2011-08-03 | 中国科学院宁波材料技术与工程研究所 | Iso-poly(sulfide-imide) and preparation method thereof |
| CN101400721B (en) * | 2006-03-16 | 2011-12-28 | 阿尔特纳电绝缘有限公司 | catalysis of polyimide curing |
| US9777118B2 (en) | 2014-04-15 | 2017-10-03 | Sabic Global Technologies B.V. | Methods of manufacture of salts of hydroxy-substituted aromatic compounds and polyetherimides |
| US10457778B2 (en) | 2014-04-15 | 2019-10-29 | Sabic Global Technologies B.V. | Methods of manufacture of polyetherimides |
| CN113637164A (en) * | 2021-08-03 | 2021-11-12 | 哈尔滨工业大学（威海） | Preparation method of novel amphiphilic biphenyl polyimide additive |
| US11220480B2 (en) | 2016-12-31 | 2022-01-11 | Shpp Global Technologies B.V. | Synthesis of reactive intermediates for polyetherimides, and uses thereof |
-
2002
- 2002-07-09 CN CNB021238979A patent/CN1169864C/en not_active Expired - Fee Related
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1298766C (en) * | 2005-06-20 | 2007-02-07 | 四川大学 | Polyarylene imide sulfide sulfone and its preparation method |
| CN101400721B (en) * | 2006-03-16 | 2011-12-28 | 阿尔特纳电绝缘有限公司 | catalysis of polyimide curing |
| CN101392055B (en) * | 2007-09-18 | 2011-08-03 | 中国科学院宁波材料技术与工程研究所 | Iso-poly(sulfide-imide) and preparation method thereof |
| US9777118B2 (en) | 2014-04-15 | 2017-10-03 | Sabic Global Technologies B.V. | Methods of manufacture of salts of hydroxy-substituted aromatic compounds and polyetherimides |
| US10457778B2 (en) | 2014-04-15 | 2019-10-29 | Sabic Global Technologies B.V. | Methods of manufacture of polyetherimides |
| US11130843B2 (en) | 2014-04-15 | 2021-09-28 | Shpp Global Technologies B.V. | Methods of manufacture of polyetherimides |
| US11220480B2 (en) | 2016-12-31 | 2022-01-11 | Shpp Global Technologies B.V. | Synthesis of reactive intermediates for polyetherimides, and uses thereof |
| CN113637164A (en) * | 2021-08-03 | 2021-11-12 | 哈尔滨工业大学（威海） | Preparation method of novel amphiphilic biphenyl polyimide additive |
| CN113637164B (en) * | 2021-08-03 | 2023-05-23 | 哈尔滨工业大学（威海） | Preparation method of amphiphilic biphenyl polyimide additive |
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