JP2002179691A5 - - Google Patents
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- Publication number
- JP2002179691A5 JP2002179691A5 JP2001338322A JP2001338322A JP2002179691A5 JP 2002179691 A5 JP2002179691 A5 JP 2002179691A5 JP 2001338322 A JP2001338322 A JP 2001338322A JP 2001338322 A JP2001338322 A JP 2001338322A JP 2002179691 A5 JP2002179691 A5 JP 2002179691A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- substituted
- unsubstituted
- atoms
- aromatic
- 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
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- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- 150000004696 coordination complex Chemical class 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 2
- 230000003197 catalytic effect Effects 0.000 claims 1
- 229910052759 nickel Inorganic materials 0.000 claims 1
- 150000003007 phosphonic acid derivatives Chemical class 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 125000003118 aryl group Chemical group 0.000 description 13
- 125000005842 heteroatom Chemical group 0.000 description 12
- 229910052799 carbon Inorganic materials 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 125000001931 aliphatic group Chemical group 0.000 description 7
- 125000004429 atom Chemical group 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 6
- 125000000962 organic group Chemical group 0.000 description 5
- 125000006413 ring segment Chemical group 0.000 description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 239000000460 chlorine Chemical group 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 239000011737 fluorine Chemical group 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000011630 iodine Chemical group 0.000 description 4
- 229910052740 iodine Chemical group 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Chemical group 0.000 description 4
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 3
- -1 —O— Chemical group 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 125000001302 tertiary amino group Chemical group 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- 125000002015 acyclic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10054218A DE10054218A1 (de) | 2000-11-02 | 2000-11-02 | Verfahren zur Herstellung von Alkenylphosphonsäure-Derivaten |
| DE10054218.2 | 2000-11-02 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002179691A JP2002179691A (ja) | 2002-06-26 |
| JP2002179691A5 true JP2002179691A5 (enExample) | 2007-01-25 |
| JP4518458B2 JP4518458B2 (ja) | 2010-08-04 |
Family
ID=7661834
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001338322A Expired - Fee Related JP4518458B2 (ja) | 2000-11-02 | 2001-11-02 | アルケニルホスホン酸誘導体の製造方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6534669B2 (enExample) |
| EP (1) | EP1203773B1 (enExample) |
| JP (1) | JP4518458B2 (enExample) |
| AT (1) | ATE273316T1 (enExample) |
| DE (2) | DE10054218A1 (enExample) |
| ES (1) | ES2225384T3 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3836395B2 (ja) * | 2002-05-17 | 2006-10-25 | 独立行政法人科学技術振興機構 | アルケニルリン化合物の製造方法 |
| JP3836460B2 (ja) * | 2003-09-03 | 2006-10-25 | 独立行政法人科学技術振興機構 | アルケニルリン化合物を製造する方法 |
| JP3836459B2 (ja) * | 2003-09-03 | 2006-10-25 | 独立行政法人科学技術振興機構 | アルケニルホスホン酸エステルの製造方法 |
| DE10350674A1 (de) | 2003-10-30 | 2005-06-02 | Basf Ag | Verfahren zur Herstellung eines Alkenylphosphonsäure-Derivats |
| DE10350676A1 (de) * | 2003-10-30 | 2005-06-02 | Basf Ag | Verfahren zur Herstellung eines Alkenylphosphonsäure-Derivats |
| EP2139904B1 (de) * | 2007-03-22 | 2013-10-16 | Basf Se | Verfahren zur herstellung eines alkenylphosphonsäure-derivats |
| WO2009124897A1 (de) * | 2008-04-08 | 2009-10-15 | Basf Se | Komplexverbindung, enthaltend metallatom und phosphinderivat als ligand |
| US8517100B2 (en) | 2010-05-12 | 2013-08-27 | Schlumberger Technology Corporation | Compositions and methods for cleaning a wellbore prior to cementing |
| WO2013033450A2 (en) | 2011-08-31 | 2013-03-07 | Mallinckrodt Llc | Remote assembly of targeted nanoparticles using h-phosphonate-ene/-yne hydrophosphonylation reactions |
| US10087265B2 (en) | 2014-06-03 | 2018-10-02 | Maruzen Petrochemical Co., Ltd. | Method for producing dimethyl polyvinylphosphonate and polyvinylphosphonic acid |
| EP3971193B1 (en) | 2019-11-27 | 2025-03-12 | Maruzen Petrochemical Co., Ltd. | Method for producing alkenyl phosphorus compound |
| CN119841866B (zh) * | 2023-10-16 | 2026-02-13 | 南开大学 | 一种通过镍铝催化七元膦氧化合物的合成方法 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3681481A (en) * | 1969-11-12 | 1972-08-01 | Hooker Chemical Corp | Catalytic addition of compounds having a p-h bond to acetylene |
| US3673285A (en) * | 1969-11-12 | 1972-06-27 | Hooker Chemical Corp | Preparation of vinyl organo-phosphorous compounds |
| US3972923A (en) | 1971-06-15 | 1976-08-03 | Hoechst Aktiengesellschaft | Process for the preparation of phosphonic acid dihalides |
| DE2132962C3 (de) | 1971-07-02 | 1979-11-22 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von 2-Chloräthanphosphonsäuredichlorid |
| IT1065240B (it) * | 1976-08-04 | 1985-02-25 | Stabil Bioterapico Farmachim | Procedimento di fabbricazione di fosfomicina |
| DE3001894A1 (de) | 1980-01-19 | 1981-07-23 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von vinyphophonsaeurederivaten |
| US4493803A (en) | 1981-05-22 | 1985-01-15 | Hoechst Aktiengesellschaft | Process for the preparation of vinylphosphonic acid diesters and vinylphosphonic acid |
| DE3120437A1 (de) | 1981-05-22 | 1982-12-09 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von vinylphosphonsaeure |
| US5216119A (en) * | 1990-12-03 | 1993-06-01 | Shell Oil Company | Catalyst compositions |
| US5210177A (en) * | 1991-05-31 | 1993-05-11 | Shell Oil Company | Polymerization of co/olefin with tetra ethyl diphosphine |
| US5693826A (en) * | 1995-09-14 | 1997-12-02 | Director-General Of Agency Of Industrial Science And Technology | Process for the production of unsaturated phosphonic ester |
| DE19715667A1 (de) * | 1997-04-15 | 1998-10-22 | Basf Ag | Verfahren zur Herstellung von Vinylphosphonsäure-Verbindungen |
| DE19828419A1 (de) * | 1998-06-25 | 1999-12-30 | Basf Ag | Verfahren zur Herstellung von Vinylphosphonsäure-Verbindungen |
| DE19933601A1 (de) * | 1999-03-08 | 2000-09-14 | Agency Ind Science Techn | Verfahren zur Herstellung ungesättigter Phosphonsäureester |
-
2000
- 2000-11-02 DE DE10054218A patent/DE10054218A1/de active Pending
-
2001
- 2001-10-27 DE DE50103200T patent/DE50103200D1/de not_active Expired - Lifetime
- 2001-10-27 EP EP01125713A patent/EP1203773B1/de not_active Expired - Lifetime
- 2001-10-27 AT AT01125713T patent/ATE273316T1/de not_active IP Right Cessation
- 2001-10-27 ES ES01125713T patent/ES2225384T3/es not_active Expired - Lifetime
- 2001-11-01 US US09/985,114 patent/US6534669B2/en not_active Expired - Lifetime
- 2001-11-02 JP JP2001338322A patent/JP4518458B2/ja not_active Expired - Fee Related
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