KR910011873A - 가수분해에 대해 안정한 유기포스 파이트의 제조방법 - Google Patents
가수분해에 대해 안정한 유기포스 파이트의 제조방법 Download PDFInfo
- Publication number
- KR910011873A KR910011873A KR1019900020650A KR900020650A KR910011873A KR 910011873 A KR910011873 A KR 910011873A KR 1019900020650 A KR1019900020650 A KR 1019900020650A KR 900020650 A KR900020650 A KR 900020650A KR 910011873 A KR910011873 A KR 910011873A
- Authority
- KR
- South Korea
- Prior art keywords
- process according
- radical
- amine
- acid
- carbon atoms
- Prior art date
Links
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 title claims 3
- 230000007062 hydrolysis Effects 0.000 title abstract 2
- 238000006460 hydrolysis reaction Methods 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract 5
- 150000003863 ammonium salts Chemical class 0.000 claims abstract 4
- 239000003960 organic solvent Substances 0.000 claims abstract 4
- 150000001875 compounds Chemical class 0.000 claims abstract 3
- 239000003054 catalyst Substances 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 6
- 150000003254 radicals Chemical class 0.000 claims 5
- 150000001412 amines Chemical class 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- -1 aromatic hydrocarbon radical Chemical class 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims 2
- 239000007864 aqueous solution Substances 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 229910052708 sodium Inorganic materials 0.000 claims 2
- 239000011734 sodium Substances 0.000 claims 2
- 239000000243 solution Substances 0.000 claims 2
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 229910001413 alkali metal ion Inorganic materials 0.000 claims 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 claims 1
- ZDZHCHYQNPQSGG-UHFFFAOYSA-N binaphthyl group Chemical group C1(=CC=CC2=CC=CC=C12)C1=CC=CC2=CC=CC=C12 ZDZHCHYQNPQSGG-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 229910001431 copper ion Inorganic materials 0.000 claims 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 claims 1
- 229910052740 iodine Chemical group 0.000 claims 1
- 239000011630 iodine Chemical group 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 239000003350 kerosene Substances 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 150000008301 phosphite esters Chemical class 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims 1
- 239000010409 thin film Substances 0.000 claims 1
- 238000005809 transesterification reaction Methods 0.000 claims 1
- 150000003738 xylenes Chemical class 0.000 claims 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 abstract 2
- 238000007037 hydroformylation reaction Methods 0.000 abstract 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
- C07F9/547—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
- C07F9/6571—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 oxygen atoms as the only ring hetero atoms
- C07F9/6574—Esters of oxyacids of phosphorus
- C07F9/65744—Esters of oxyacids of phosphorus condensed with carbocyclic or heterocyclic rings or ring systems
-
- 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
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/141—Esters of phosphorous acids
-
- 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
- C07F9/6571—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 oxygen atoms as the only ring hetero atoms
- C07F9/6574—Esters of oxyacids of phosphorus
- C07F9/65746—Esters of oxyacids of phosphorus the molecule containing more than one cyclic phosphorus atom
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Catalysts (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 식PX3또는(R3O) PX2(식에서 X는 염소, 브롬 또는 요오드이고 R3는 임의적으로 치환된 지방족, 고리지방족 또는 방향족 탄화수소 라디칼임)의 유기포스파이트 또는 인-할로겐 화합물을 물에 불용성 이고 유기용매에 용해되는 당량 또는 과량의 히도록시 술폰산의 암모늄염과 반응시키는 것으로 이루어지는, 가수분해에 대해 안정한 포스파이트의 제조방법.
- 제1항에 있어서, 히드록시술폰산의 암모늄염이 히드록시 술폰산의 수용액 또는 히드록시 술폰산의 수용성염의 산성화된 용액과 수불용성 유기용매내 수불용성아민의 용액과의 반응으로 수득된 생성물 형태로 사용되는 방법.
- 제2항에 있어서, 히드록시술폰산 또는 그의 수용성염이 하기식의 화합물인 방법.(MO3S)n-Y-(OH)m〔상기식에서 Y는 유기라디칼, M은 수소이온, 알칼리 금속이온 또는 식〔NP4〕4(식에서 R은 수소 및/또는 같거나 다른 직쇄 또는 분지쇄 C1-또는 C4-알킬라디칼임)의 암모늄이온 또는 알칼리토금속이온, 납이온 또는 구리이온의 등가물이며, m은 1-3의 정수이고 n은 1-4의 정수이다.
- 제2항에서 있어서, 식(MO3S)n-Y-(OH)m에서, Y는 탄소원자수 2-20의 직쇄 또는 분지쇄 포화 지방족 라디칼, 탄소원자수 5∼12의 단핵 또는 2핵 고리지방족 라디칼, 벤젠비페닐, 나프탈렌 또는 비나프틸로부터 유도된 라디칼, 벤질라디칼, 톨루엔, 에티벤젠, 또는 크실렌 이성질체로 부터 유도된 라디칼 또는 포화 또는 불포화질소함유 5-또는 6-원고리, 특히 피리딘으로 부터 유도된 라디칼인 방법.
- 제2항 내지 4항중 어느한항에 있어서, 히드록시술폰산의 염의 수용액의 H2SO4, HCL, HNO, H3PO4, HF 또는 HBF4에 의해 산성화되는 방법.
- 제2항 내지 5항중 어느한항에 있어서, 술폰산 다량 당 0.8-1.2몰의 아민이 사용되는 방법.
- 제1항 내지 6항중 어느 한항에 있어서, 유기용매에 용해되는 암모늄염이 전체 탄소원자수 10-60, 바람직하게는 12-36을 갖는 수불용성 직쇄 또는 분지쇄 지방족 아민으로 부터 유도되는 방법.
- 제2항 내지 7항중 어느 한항에 있어서, 톨루엔 또는 케로센형 탄화수소 분획이 아민에 대한 용매로서 사용되는 방법.
- 제1 내지 8항중 어느 한항에 있어서, 유기 포스파이트의 반응이 촉매로서 나트륨, 아민, 나트륨 알코올레이트, 알루미늄 클로라이드, 티탄산에스테르 또는 아인산 디알킬 에스테르 존재하에 수행되는 방법.
- 제1내지 9항중 어느 한항에 있어서, 트랜스 에스테르화 반응에 의해 유리된 페놀이 박막 증발기를 사용하여 연속적으로 진공 증류 제거되는 방법※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3942787.0 | 1989-12-23 | ||
DEP3942787.0 | 1989-12-23 | ||
DE3942787A DE3942787A1 (de) | 1989-12-23 | 1989-12-23 | Verfahren zur herstellung hydrolysestabiler organischer phosphite |
Publications (2)
Publication Number | Publication Date |
---|---|
KR910011873A true KR910011873A (ko) | 1991-08-07 |
KR940001061B1 KR940001061B1 (ko) | 1994-02-12 |
Family
ID=6396314
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900020650A KR940001061B1 (ko) | 1989-12-23 | 1990-12-14 | 가수분해에 대해 안정한 유기포스파이트의 제조방법 |
Country Status (10)
Country | Link |
---|---|
US (1) | US5126475A (ko) |
EP (1) | EP0435071B1 (ko) |
JP (1) | JPH07110868B2 (ko) |
KR (1) | KR940001061B1 (ko) |
AT (1) | ATE114314T1 (ko) |
AU (1) | AU629079B2 (ko) |
BR (1) | BR9006501A (ko) |
CA (1) | CA2032371C (ko) |
DE (2) | DE3942787A1 (ko) |
ES (1) | ES2066945T3 (ko) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5292785A (en) * | 1992-05-05 | 1994-03-08 | Ciba-Geigy Corporation | Bis-phosphite stabilized compositions |
US5391799A (en) * | 1992-05-05 | 1995-02-21 | Ciba-Geigy Corporation | Process for the preparation 6-chloro-2,4,8,10-tetra-butyldibenzo[d,f][1,3,2]dioxaphoshepin |
US5786497A (en) * | 1997-08-29 | 1998-07-28 | General Electric Company | Process for the preparation of phosphites |
US5919966A (en) * | 1998-03-26 | 1999-07-06 | General Electric Company | Process for the preparation of spiro bis-phosphites |
US5917076A (en) * | 1998-04-16 | 1999-06-29 | General Electric Company | Process for the preparation of spiro bis-phosphites using finely ground pentaerythritol |
US6426429B1 (en) | 2000-08-11 | 2002-07-30 | General Electric Company | Process for the preparation of hindered phosphites |
US6504065B1 (en) | 2000-09-29 | 2003-01-07 | General Electric Company | Method of making metal salts of 2,4,6-tri-t-butylphenol |
DE10240050B3 (de) * | 2002-08-30 | 2004-01-22 | Bayer Ag | Verfahren zur kombinierten Herstellung von Diethylphosphit und Ethylchlorid |
EP2014752A1 (en) | 2007-06-23 | 2009-01-14 | Cognis IP Management GmbH | Process for the manufacture of saturated fatty acid esters in the presence of a homogeneous complex of a Group VIII metal and a sulfonated phosphite |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2860898D1 (en) * | 1977-08-08 | 1981-11-05 | Ciba Geigy Ag | Process for the preparation of triarylphosphites |
FR2465740A1 (fr) * | 1978-05-31 | 1981-03-27 | Cellophane Sa | Nouveaux derives du naphtalene diol-2,3 |
-
1989
- 1989-12-23 DE DE3942787A patent/DE3942787A1/de not_active Withdrawn
-
1990
- 1990-12-12 DE DE59007762T patent/DE59007762D1/de not_active Expired - Fee Related
- 1990-12-12 EP EP90123911A patent/EP0435071B1/de not_active Expired - Lifetime
- 1990-12-12 ES ES90123911T patent/ES2066945T3/es not_active Expired - Lifetime
- 1990-12-12 AT AT90123911T patent/ATE114314T1/de not_active IP Right Cessation
- 1990-12-14 KR KR1019900020650A patent/KR940001061B1/ko not_active IP Right Cessation
- 1990-12-14 CA CA002032371A patent/CA2032371C/en not_active Expired - Fee Related
- 1990-12-17 JP JP2402868A patent/JPH07110868B2/ja not_active Expired - Lifetime
- 1990-12-20 BR BR909006501A patent/BR9006501A/pt not_active Application Discontinuation
- 1990-12-21 US US07/632,465 patent/US5126475A/en not_active Expired - Fee Related
- 1990-12-21 AU AU68368/90A patent/AU629079B2/en not_active Ceased
Also Published As
Publication number | Publication date |
---|---|
US5126475A (en) | 1992-06-30 |
AU629079B2 (en) | 1992-09-24 |
AU6836890A (en) | 1991-06-27 |
KR940001061B1 (ko) | 1994-02-12 |
BR9006501A (pt) | 1991-10-01 |
CA2032371C (en) | 1995-04-04 |
EP0435071A3 (en) | 1991-09-18 |
DE3942787A1 (de) | 1991-06-27 |
ATE114314T1 (de) | 1994-12-15 |
DE59007762D1 (de) | 1995-01-05 |
JPH06239878A (ja) | 1994-08-30 |
EP0435071A2 (de) | 1991-07-03 |
JPH07110868B2 (ja) | 1995-11-29 |
ES2066945T3 (es) | 1995-03-16 |
EP0435071B1 (de) | 1994-11-23 |
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