KR900701802A - Method for preparing isomerized trisaryloxycyclotriphosphazene polymer precursors and intermediates - Google Patents
Method for preparing isomerized trisaryloxycyclotriphosphazene polymer precursors and intermediatesInfo
- Publication number
- KR900701802A KR900701802A KR1019900700385A KR900700385A KR900701802A KR 900701802 A KR900701802 A KR 900701802A KR 1019900700385 A KR1019900700385 A KR 1019900700385A KR 900700385 A KR900700385 A KR 900700385A KR 900701802 A KR900701802 A KR 900701802A
- Authority
- KR
- South Korea
- Prior art keywords
- tris
- cyclotriphosphazene
- phenoxy
- nitrophenoxy
- nitrophenol
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 8
- 239000000543 intermediate Substances 0.000 title 1
- 229920000642 polymer Polymers 0.000 title 1
- 239000002243 precursor Substances 0.000 title 1
- -1 4-nitrophenol, alkali metal phenol salts Chemical class 0.000 claims description 8
- AWASCCZQTBFRIB-UHFFFAOYSA-N 2,4,6-tris(4-nitrophenoxy)-2,4,6-triphenoxy-1,3,5-triaza-2lambda5,4lambda5,6lambda5-triphosphacyclohexa-1,3,5-triene Chemical compound [N+](=O)([O-])C1=CC=C(OP2(=NP(=NP(=N2)(OC2=CC=CC=C2)OC2=CC=C(C=C2)[N+](=O)[O-])(OC2=CC=CC=C2)OC2=CC=C(C=C2)[N+](=O)[O-])OC2=CC=CC=C2)C=C1 AWASCCZQTBFRIB-UHFFFAOYSA-N 0.000 claims description 5
- 239000007983 Tris buffer Substances 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 4
- 239000003960 organic solvent Substances 0.000 claims 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- MIUNCOSIUQDUHS-UHFFFAOYSA-N C(C=C1)=CC=C1OP([N]P([N]1)OC2=CC=CC=C2)[N]P1OC1=CC=CC=C1 Chemical compound C(C=C1)=CC=C1OP([N]P([N]1)OC2=CC=CC=C2)[N]P1OC1=CC=CC=C1 MIUNCOSIUQDUHS-UHFFFAOYSA-N 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- NNHKDHFEUKGYSB-UHFFFAOYSA-N 2,4,6-trichloro-2,4,6-triphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(Cl)(OC=2C=CC=CC=2)=NP(Cl)(OC=2C=CC=CC=2)=NP=1(Cl)OC1=CC=CC=C1 NNHKDHFEUKGYSB-UHFFFAOYSA-N 0.000 claims 1
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- UBIJTWDKTYCPMQ-UHFFFAOYSA-N hexachlorophosphazene Chemical compound ClP1(Cl)=NP(Cl)(Cl)=NP(Cl)(Cl)=N1 UBIJTWDKTYCPMQ-UHFFFAOYSA-N 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 claims 1
- 229910003446 platinum oxide Inorganic materials 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical group [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 claims 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
- C07F9/65812—Cyclic phosphazenes [P=N-]n, n>=3
- C07F9/65815—Cyclic phosphazenes [P=N-]n, n>=3 n = 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
Abstract
내용 없음No content
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.
제1도는 본 발명에 따른 트리스(4-니트로페녹시) 트리스 (페녹시)시클로트리포스파젠(Ⅲ)의 제조에 관한 제1방법의 반응기구를 설명한다. 제2도는 본 발명에 따른 트리스(4-니트로페녹시) 트리스(페녹시) 시클로트리포스파젠(Ⅲ*)의 제조에 관한 제2방법의 반응 기구을 설명한다. 제3도는 본 발명에 따른 트리스(4-니트로메톡시) 트리스(페녹시) 시클로트리포스파젠(Ⅲ*)의 제조에 관한 제3방법의 반응 기구를 설명한다.1 illustrates a reactor mechanism of a first method for the preparation of tris (4-nitrophenoxy) tris (phenoxy) cyclotriphosphazene (III) according to the present invention. 2 illustrates the reaction mechanism of the second method for the preparation of tris (4-nitrophenoxy) tris (phenoxy) cyclotriphosphazene (III * ) according to the present invention. 3 illustrates the reaction mechanism of the third method for preparing tris (4-nitromethoxy) tris (phenoxy) cyclotriphosphazene (III * ) according to the present invention.
Claims (7)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21027488A | 1988-06-23 | 1988-06-23 | |
US210,274 | 1988-06-23 | ||
PCT/US1989/002600 WO1989012639A1 (en) | 1988-06-23 | 1989-06-20 | Process for preparing isomeric trisaryloxycyclotriphosphazene polymer precursors and intermediates |
Publications (1)
Publication Number | Publication Date |
---|---|
KR900701802A true KR900701802A (en) | 1990-12-04 |
Family
ID=22782273
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900700385A KR900701802A (en) | 1988-06-23 | 1989-06-20 | Method for preparing isomerized trisaryloxycyclotriphosphazene polymer precursors and intermediates |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0380616A4 (en) |
JP (1) | JPH02502731A (en) |
KR (1) | KR900701802A (en) |
AU (1) | AU3855689A (en) |
WO (1) | WO1989012639A1 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4635157B2 (en) * | 2004-09-27 | 2011-02-16 | 株式会社伏見製薬所 | Method for producing cyclotriphosphazene derivative |
JP4635155B2 (en) * | 2004-09-27 | 2011-02-16 | 株式会社伏見製薬所 | Method for producing cyclotriphosphazene derivative |
JP4635156B2 (en) * | 2004-09-27 | 2011-02-16 | 株式会社伏見製薬所 | Method for producing cyclotriphosphazene derivative |
US20080091050A1 (en) * | 2005-01-21 | 2008-04-17 | Asahi Kasei Chemical Corporation | Process For Producing Phosphonitrilic Acid Ester |
CN102358748B (en) * | 2011-07-15 | 2013-10-16 | 云南师范大学 | Star chain transferring agent using cyclotriphosphazene as nucleus, and preparation method and application thereof |
CN103435653B (en) * | 2013-08-08 | 2015-12-02 | 清远市普塞呋磷化学有限公司 | A kind of preparation method of hexaphenoxycyclotriphosphazene |
CN105153366B (en) * | 2015-09-30 | 2017-07-28 | 杭州方圆塑机股份有限公司 | A kind of preparation method of flame-retardant modified polyvinyl acetate for expanded polystyrene bead |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4600791A (en) * | 1983-12-12 | 1986-07-15 | Borg-Warner Chemicals, Inc. | Process for preparation of phosphazene esters |
US4634759A (en) * | 1984-04-11 | 1987-01-06 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Fire and heat resistant laminating resins based on maleimido substituted aromatic cyclotriphosphazene polymer |
US4772722A (en) * | 1986-09-10 | 1988-09-20 | Hercules Incorporated | Nadimido-substituted cyclophosphazene |
-
1989
- 1989-06-20 AU AU38556/89A patent/AU3855689A/en not_active Abandoned
- 1989-06-20 WO PCT/US1989/002600 patent/WO1989012639A1/en not_active Application Discontinuation
- 1989-06-20 KR KR1019900700385A patent/KR900701802A/en not_active Application Discontinuation
- 1989-06-20 EP EP19890907955 patent/EP0380616A4/en not_active Withdrawn
- 1989-06-20 JP JP1507357A patent/JPH02502731A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
JPH02502731A (en) | 1990-08-30 |
WO1989012639A1 (en) | 1989-12-28 |
EP0380616A4 (en) | 1990-09-05 |
EP0380616A1 (en) | 1990-08-08 |
AU3855689A (en) | 1990-01-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E601 | Decision to refuse application |