CN1986526A - Preparing process of 4,4-(4-aminophenoxy) diphenyl sulfone - Google Patents
Preparing process of 4,4-(4-aminophenoxy) diphenyl sulfone Download PDFInfo
- Publication number
- CN1986526A CN1986526A CN 200510111699 CN200510111699A CN1986526A CN 1986526 A CN1986526 A CN 1986526A CN 200510111699 CN200510111699 CN 200510111699 CN 200510111699 A CN200510111699 A CN 200510111699A CN 1986526 A CN1986526 A CN 1986526A
- Authority
- CN
- China
- Prior art keywords
- sulfobenzide
- mixed solvent
- amino
- nitrophenoxy
- hydrazine hydrate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The present invention discloses preparation process of 4, 4'-(4-amino phenoxy) diphenyl sulfone. The present invention prepares 4, 4'-(4-amino phenoxy) diphenyl sulfone at normal pressure by using 4, 4'-(4-nitro phenoxy) diphenyl sulfone as main material and hydrazine hydrate as reductant, and through reduction reaction in mixed solvent in the presence of catalyst. The process has 4, 4'-(4-amino phenoxy) diphenyl sulfone product purity up to 98.5 %, yield over 90 % and smelting point of 194.1-194.8 deg.c. Compared with available technology, the present invention has the advantages of reaction at normal pressure, high operation safety, etc and is suitable for industrial production.
Description
Technical field
The present invention relates to a kind of preparation method's of 4,4 '-(4-amino-benzene oxygen) sulfobenzide improvement.
Background technology
4,4 '-(4-amino-benzene oxygen) sulfobenzide is a kind of intermediate of synthetic resins, can be used as the intermediate of synthetic bimaleimide resin especially, good effect is arranged aspect the resin property improving.
Its structural formula is as follows:
In the existing document, U.S. Pat .3,988,374 reported method are with 4,4 '-(4-nitrophenoxy) sulfobenzide is a raw material, through synthetic 4,4 '-(4-amino-benzene oxygen) sulfobenzide of shortening.The method of this patent report is synthesized in autoclave, and complex operation has certain danger, and industrial prospect is undesirable.
Beijing Chemical Engineering College's journal (natural science edition) 19 (2) 32-37 1992 have reported with p-aminophenol and dichloro diphenylsulfone reaction, make 4,4 '-(4-amino-benzene oxygen) sulfobenzide, through acid-base neutralisation method purifying, obtain the method for 4,4 ' of purity 98%-(4-amino-benzene oxygen) sulfobenzide product.This method cost height, shade deviation is difficult to reach the requirement of application.
Summary of the invention
The technical problem that the present invention solves provides a kind of preparation method of 4,4 '-(4-amino-benzene oxygen) sulfobenzide, overcoming cost height in the prior art, and shade deviation, reaction under high pressure is dangerous big, the deficiency of complex operation.
Technical conceive of the present invention is such:
With 4,4 '-(4-nitrophenoxy) sulfobenzide is a raw material, is reductive agent with the hydrazine hydrate, in mixed solvent, carries out reduction reaction under the existence of catalyzer, thereby can prepare said 4,4 '-(4-amino-benzene oxygen) sulfobenzide under normal pressure.
Technical scheme of the present invention:
With 4,4 '-(4-nitrophenoxy) sulfobenzide, gac and catalyzer add in the mixed solvent, drip the reductive agent hydrazine hydrate under the condition of normal pressure, 65-90 ℃, react 2-5 hour, from reaction product, collect target product 4,4 '-(4-amino-benzene oxygen) sulfobenzide.
Reaction formula of the present invention is as follows:
The said catalyzer of the present invention is a kind of in six Ferric Chloride Hydrateds or the 2%-5% palladium/carbon, preferred six Ferric Chloride Hydrateds, and reactant 4,4 '-(4-nitrophenoxy) sulfobenzide and catalyst quality are than being 100-300: 1.
Mixed solvent of the present invention is mixed by ethanol and dimethyl formamide (DMF) and forms, and according to 1: the volume ratio of 1-2 is prepared, reactant 4, and the weightmeasurement ratio of 4 '-(4-nitrophenoxy) sulfobenzide and mixed solvent is 1: 3-10;
The content of reductive agent hydrazine hydrate of the present invention is 20wt%-80wt%, and the content of preferred hydrazine hydrate is 80wt%, reactant 4, and the mol ratio of 4 '-(4-nitrophenoxy) sulfobenzide and reductive agent hydrazine hydrate is 1: 2-6;
According to the present invention, from reaction product, collect target product 4,4 '-(4-amino-benzene oxygen) sulfobenzide and comprise the steps: to filter, steam and remove mixed solvent, in water, separate out crystal, be target product of the present invention.
4,4 '-(4-amino-benzene oxygen) the sulfobenzide purity that obtains with preparation method of the present invention reaches more than 99%, and productive rate is greater than 90%, and fusing point is 194.1-194.8 ℃, identifies the structure of product with nucleus magnetic resonance.
Raw material 4,4 ' used in the present invention-(4-nitrophenoxy) sulfobenzide can prepare by the method for EP 0537589 A2.
The present invention is reflected under the normal pressure and carries out compared with prior art, simple and safe operation, and the good product purity that obtains, cost is low, and color and luster is white, is suitable for suitability for industrialized production.
Embodiment
The invention will be further described below by embodiment, but embodiment does not limit protection scope of the present invention.
Embodiment 1
In the reactor that has heating, stirring, thermometer, add 196.8g (0.40mol) 4 respectively, 4 '-(4-nitrophenoxy) sulfobenzide, the 40g gac, 1g six Ferric Chloride Hydrateds, the mixed solvent of 1500ml ethanol and dimethyl formamide (DMF) (volume ratio 1: 2), stir under the room temperature, heating gradually, temperature of reaction is controlled at 70-80 ℃, splash into 100.0g (1.6mol) 80% hydrazine hydrate in 2 hours, continuation obtains 4,4 '-(4-amino-benzene oxygen) sulfobenzide 80-90 ℃ of reaction 4 hours.Steam mixed solvent 1000ml (reclaiming the back reuses) with rotatory evaporator behind the reacting liquid filtering, be cooled to room temperature, add 400ml water, separate out crystal, filter, dry, obtain 4,4 '-(4-amino-benzene oxygen) sulfobenzide 161.9g of white, productive rate 93.7%, purity 99.23% (HPLC), fusing point: 194.0-194.3 ℃ (literature value: 194-195 ℃).
Embodiment 2
In the reactor that has heating, stirring, thermometer, add 196.8g (0.40mol) 4 respectively, 4 '-(4-nitrophenoxy) sulfobenzide, 40g gac, 1g 5% palladium/carbon, the mixed solvent of 1500ml ethanol and dimethyl formamide (DMF) (volume ratio 1: 1.8), stir under the room temperature, heating gradually, temperature of reaction is controlled at 70-80 ℃, splash into 100.0g (1.6mol) 80% hydrazine hydrate in 2 hours, continuation obtains 4,4 '-(4-amino-benzene oxygen) sulfobenzide 80-90 ℃ of reaction 4 hours.Steam mixed solvent 1000ml with rotatory evaporator behind the reacting liquid filtering, be cooled to room temperature, add 400ml water, separate out crystal, filter, drying obtains 4,4 '-(4-amino-benzene oxygen) white sulfobenzide 158.7g, productive rate 91.8%; Purity 99.03% (HPLC); Fusing point: 194.1-194.9 ℃.
Embodiment 3
In the reactor that has heating, stirring, thermometer, add 196.8g (0.40mol) 4 respectively, 4,-(4-nitrophenoxy) sulfobenzide, the 40g gac, 1g six Ferric Chloride Hydrateds, the mixed solvent of 1500ml ethanol and dimethyl formamide (DMF) (volume ratio 1: 1.2), stir under the room temperature, heating gradually, temperature of reaction is controlled at 70-80 ℃, splashes into 62.5g (1.0mol) 80% hydrazine hydrate in 1.5 hours, continues 80-90 ℃ of reaction 4 hours, obtain 4,4 '-(4-amino-benzene oxygen) sulfobenzide.Steam mixed solvent 1000ml with rotatory evaporator behind the reacting liquid filtering, be cooled to room temperature, add 400ml water, separate out crystal, filter, drying obtains 4,4 '-(4-amino-benzene oxygen) white sulfobenzide 157.9g, productive rate 91.3%; Purity 98.76% (HPLC); Fusing point: 193.7-194.1 ℃.
Claims (9)
1. one kind 4, the preparation method of 4 '-(4-amino-benzene oxygen) sulfobenzide comprises the steps:
With 4,4 '-(4-nitrophenoxy) sulfobenzide, gac and catalyzer add in the mixed solvent, at normal pressure, drip the reductive agent hydrazine hydrate under 65-90 ℃ the condition, reacted 2-5 hour, and from reaction product, collected target product 4,4 '-(4-amino-benzene oxygen) sulfobenzide.
2. method according to claim 1 is characterized in that, said catalyzer is a kind of in six Ferric Chloride Hydrateds or the 2%-5% palladium/carbon.
3. method according to claim 1 is characterized in that, said mixed solvent is that ethanol and dimethyl formamide mix composition.
4. method according to claim 1 is characterized in that the content of said reductive agent hydrazine hydrate is 20wt%-80wt%.
5. method according to claim 5 is characterized in that the content of said reductive agent hydrazine hydrate is 80wt%.
6. according to each described method of claim 1-6, it is characterized in that, reactant 4, the weightmeasurement ratio of 4 '-(4-nitrophenoxy) sulfobenzide and mixed solvent is 1: 3-10, mixed solvent ethanol is with 1 with DMF: the 1-2 volume ratio is mixed composition.
7. according to each described method of claim 1-6, it is characterized in that, reactant 4,4 '-(4-nitrophenoxy) sulfobenzide is 100-300 with the catalyst quality ratio: 1.
8. according to each described method of claim 1-6, it is characterized in that, reactant 4, the mol ratio of 4 '-(4-nitrophenoxy) sulfobenzide and reductive agent hydrazine hydrate is 1: 2-6.
9. method according to claim 1 is characterized in that, collects target product 4,4 '-(4-amino-benzene oxygen) sulfobenzide and comprise the steps: to filter from reaction product, steams and removes mixed solvent, separates out crystal in water, is target product of the present invention.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB200510111699XA CN100494173C (en) | 2005-12-20 | 2005-12-20 | Preparing process of 4,4-(4-aminophenoxy) diphenyl sulfone |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB200510111699XA CN100494173C (en) | 2005-12-20 | 2005-12-20 | Preparing process of 4,4-(4-aminophenoxy) diphenyl sulfone |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1986526A true CN1986526A (en) | 2007-06-27 |
| CN100494173C CN100494173C (en) | 2009-06-03 |
Family
ID=38183482
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB200510111699XA Expired - Fee Related CN100494173C (en) | 2005-12-20 | 2005-12-20 | Preparing process of 4,4-(4-aminophenoxy) diphenyl sulfone |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100494173C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101245041B (en) * | 2008-03-21 | 2010-12-01 | 东华大学 | Process for producing 4,4'-bis(2,4-diaminophenyloxy)diphenyl sulfone |
-
2005
- 2005-12-20 CN CNB200510111699XA patent/CN100494173C/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101245041B (en) * | 2008-03-21 | 2010-12-01 | 东华大学 | Process for producing 4,4'-bis(2,4-diaminophenyloxy)diphenyl sulfone |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100494173C (en) | 2009-06-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN103140465B (en) | The method of synthesis 2-methoxymethyl-Isosorbide-5-Nitrae-phenylenediamine | |
| CN101891606B (en) | New method for synthesizing rhodium caprylate (II) | |
| CN101402610A (en) | Synthesis method of 4-(3-chlorine-4-fluorobenzene amino)-7-methoxy-6-[3-(4-morpholinyl)-propoxy] quinoline | |
| CN108503554A (en) | A kind of synthetic method of bricalin | |
| CN87107214A (en) | High purity 4,6-diaminostilbene, the preparation method of 3-dihydroxy-benzene | |
| CN100494173C (en) | Preparing process of 4,4-(4-aminophenoxy) diphenyl sulfone | |
| CN101239919A (en) | Method for synthesizing aromatic diamines monomer | |
| CN110560150A (en) | Catalyst for preparing methyl acetate by methanol carbonylation and application thereof | |
| CN102603623A (en) | Method for preparing high-purity roflumilast | |
| CN101914064B (en) | Method for preparing sulfachlororyridazine sodium | |
| CN1472193A (en) | Preparation of 2,2-bi-[4-(4-aminophenoxy)phenyl]propane | |
| CN102976961A (en) | Method for preparing methoxamine hydrochloride | |
| CN110963946B (en) | Preparation method of sodium methyl taurate | |
| CN101012178A (en) | Method of preparing 3-aminophthalic acid from 3-nitrophthalic acid | |
| CN106674135A (en) | Uracil synthesizing method | |
| CN100368383C (en) | Fluorine containing asymmetric aromatic ether diamine and preparation and use thereof | |
| CN101429117A (en) | Process for producing 2, 4, 6-trichlorobenzoic acid | |
| CN102942533B (en) | Preparation method of 4-(5-amino-6-hydroxy-2-benzoxazolyl) benzoic acid (ABA) | |
| CN101830845A (en) | Synthesis method of 5-chloro-2,3-dihydroxyl pyridine | |
| CN106854200A (en) | The preparation method of Ceritinib and its intermediate | |
| CN108276328A (en) | A kind of preparation method of Sorafenib | |
| CN105254614B (en) | A kind of synthetic method of ZD6474 compound | |
| CN102381957A (en) | Method for preparing acetic acid ruthenium | |
| CN109503499A (en) | A kind of Fan get Ta Ni intermediate and preparation method thereof | |
| CN110423492A (en) | The method of the indigo white salting liquid of preparation method and continuous production of indigo white salting liquid |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20090603 Termination date: 20131220 |