SE0600484L - Process for Preparation of a Bisphthalonitrile Monomer - Google Patents
Process for Preparation of a Bisphthalonitrile MonomerInfo
- Publication number
- SE0600484L SE0600484L SE0600484A SE0600484A SE0600484L SE 0600484 L SE0600484 L SE 0600484L SE 0600484 A SE0600484 A SE 0600484A SE 0600484 A SE0600484 A SE 0600484A SE 0600484 L SE0600484 L SE 0600484L
- Authority
- SE
- Sweden
- Prior art keywords
- bis
- benzene
- yielded
- subjecting
- reaction
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/0622—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms
- C08G73/0638—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms with at least three nitrogen atoms in the ring
- C08G73/065—Preparatory processes
- C08G73/0655—Preparatory processes from polycyanurates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
- C08G65/4012—Other compound (II) containing a ketone group, e.g. X-Ar-C(=O)-Ar-X for polyetherketones
- C08G65/4031—(I) or (II) containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/48—Polymers modified by chemical after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Dislosed is a process for production of a bis-phthalonitrile monomer having an oligophenyl ether spacer chain, said bis-phthalonitrile of Formula (I) wherein n is 2. The process comprises (i) subjecting a 3-alkoxyphenol to reaction with a m-dihalobenzene in the presence of a base and a catalyst composition comprising a copper salt and a ligand whereby a 1,3-bis (3-alkoxyphenoxy) benzene is yielded, (ii) subjecting yielded 1 ,3-bis (3-alkoxyphenoxy) benzene to reaction with a dealkylating agent yielding 1 ,3-bis(3- hydroxyphenoxy)benzene, and (iii) subjecting yielded 1,3-bis (3-hydroxyphenoxy) benzene to reaction with a 4-nitrophthalonitrile in presence of a base yielding 1,3-bis [3-(3,4-dicyano- phenoxy)phenoxy]benzene.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE0600484A SE530059C2 (en) | 2006-03-06 | 2006-03-06 | Process for Preparation of a Bisphthalonitrile Monomer |
KR1020087023461A KR20080098435A (en) | 2006-03-06 | 2007-03-05 | Process for production of a bis-phthalonitrile monomer |
CNA2007800079079A CN101395201A (en) | 2006-03-06 | 2007-03-05 | Process for production of a bis-phthalonitrile monomer |
PCT/SE2007/000210 WO2007102766A1 (en) | 2006-03-06 | 2007-03-05 | Process for production of a bis-phthalonitrile monomer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE0600484A SE530059C2 (en) | 2006-03-06 | 2006-03-06 | Process for Preparation of a Bisphthalonitrile Monomer |
Publications (2)
Publication Number | Publication Date |
---|---|
SE0600484L true SE0600484L (en) | 2007-09-07 |
SE530059C2 SE530059C2 (en) | 2008-02-19 |
Family
ID=38475139
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE0600484A SE530059C2 (en) | 2006-03-06 | 2006-03-06 | Process for Preparation of a Bisphthalonitrile Monomer |
Country Status (4)
Country | Link |
---|---|
KR (1) | KR20080098435A (en) |
CN (1) | CN101395201A (en) |
SE (1) | SE530059C2 (en) |
WO (1) | WO2007102766A1 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102993070A (en) * | 2012-12-04 | 2013-03-27 | 四川大学 | Aromatic diamine containing phthalonitrile side group and synthesis method and application thereof |
CN103408755A (en) * | 2013-07-09 | 2013-11-27 | 中国船舶重工集团公司第七二五研究所 | Low-viscosity cyano resin monomer and polymer, and preparation method thereof |
EP3436428A1 (en) * | 2016-03-31 | 2019-02-06 | 3M Innovative Properties Company | Bisphenol m diphthalonitrile ether resin, bisphenol p diphthalonitrile ether resin, methods of making same, resin blends, and two component systems |
CN106046360A (en) * | 2016-04-15 | 2016-10-26 | 电子科技大学 | Aromatic nitrile polymer and preparation method thereof |
WO2018018070A1 (en) * | 2016-07-25 | 2018-02-01 | The Boeing Company | Epoxy resin |
EP3487904A4 (en) * | 2016-07-25 | 2020-06-10 | The Boeing Company | Epoxy resin |
KR102218559B1 (en) | 2018-08-28 | 2021-02-22 | 주식회사 엘지화학 | Phthalonitrile-based resin with improved impact strength |
CN111479885B (en) | 2018-09-21 | 2022-05-27 | 株式会社Lg化学 | Curable resin composition comprising phthalonitrile oligomer and prepolymer thereof |
RU2708399C1 (en) * | 2018-12-03 | 2019-12-06 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Ивановский государственный химико-технологический университет" (ИГХТУ) | 4,4'-(((1,4-phenylenebis(oxy))bis(4,1-phenylene))bis(oxy))diphtalonitrile |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6756470B2 (en) * | 2002-04-26 | 2004-06-29 | The United States Of America As Represented By The Secretary Of The Navy | Oligomeric hydroxy arylether phthalonitiles and synthesis thereof |
-
2006
- 2006-03-06 SE SE0600484A patent/SE530059C2/en not_active IP Right Cessation
-
2007
- 2007-03-05 CN CNA2007800079079A patent/CN101395201A/en active Pending
- 2007-03-05 WO PCT/SE2007/000210 patent/WO2007102766A1/en active Application Filing
- 2007-03-05 KR KR1020087023461A patent/KR20080098435A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
KR20080098435A (en) | 2008-11-07 |
CN101395201A (en) | 2009-03-25 |
WO2007102766A1 (en) | 2007-09-13 |
SE530059C2 (en) | 2008-02-19 |
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Legal Events
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NUG | Patent has lapsed |