IE43253B1 - Production of beta-halogenformyl-ethyl phosphinic acid halides - Google Patents
Production of beta-halogenformyl-ethyl phosphinic acid halidesInfo
- Publication number
- IE43253B1 IE43253B1 IE1458/76A IE145876A IE43253B1 IE 43253 B1 IE43253 B1 IE 43253B1 IE 1458/76 A IE1458/76 A IE 1458/76A IE 145876 A IE145876 A IE 145876A IE 43253 B1 IE43253 B1 IE 43253B1
- Authority
- IE
- Ireland
- Prior art keywords
- phosphinic acid
- beta
- acid halide
- ethyl
- reaction zone
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- 238000006243 chemical reaction Methods 0.000 claims abstract description 37
- 238000000034 method Methods 0.000 claims abstract description 27
- -1 phosphinic acid halides Chemical class 0.000 claims abstract description 17
- 239000000463 material Substances 0.000 claims abstract description 16
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000460 chlorine Substances 0.000 claims abstract description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 7
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims abstract description 7
- 239000000155 melt Substances 0.000 claims abstract description 6
- 239000007858 starting material Substances 0.000 claims abstract description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims abstract description 4
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 4
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000005843 halogen group Chemical group 0.000 claims abstract description 3
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 2
- KNOCWCOUBNZCOC-UHFFFAOYSA-N 3-[chloro(methyl)phosphoryl]-2-methylpropanoyl chloride Chemical compound ClC(=O)C(C)CP(C)(Cl)=O KNOCWCOUBNZCOC-UHFFFAOYSA-N 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 239000000047 product Substances 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- SGGKZWABPPXBNE-UHFFFAOYSA-N 3-[chloro(methyl)phosphoryl]propanoyl chloride Chemical compound CP(Cl)(=O)CCC(Cl)=O SGGKZWABPPXBNE-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- JUODZJFVOZRRQW-UHFFFAOYSA-N 3-[chloro(phenyl)phosphoryl]propanoyl chloride Chemical compound ClC(=O)CCP(Cl)(=O)C1=CC=CC=C1 JUODZJFVOZRRQW-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- CDPKWOKGVUHZFR-UHFFFAOYSA-N dichloro(methyl)phosphane Chemical compound CP(Cl)Cl CDPKWOKGVUHZFR-UHFFFAOYSA-N 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- JHNJGLVSPIMBLD-UHFFFAOYSA-N dichloro(ethyl)phosphane Chemical compound CCP(Cl)Cl JHNJGLVSPIMBLD-UHFFFAOYSA-N 0.000 description 2
- IMDXZWRLUZPMDH-UHFFFAOYSA-N dichlorophenylphosphine Chemical compound ClP(Cl)C1=CC=CC=C1 IMDXZWRLUZPMDH-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- KJKWGCTWYJCDHP-UHFFFAOYSA-N 1-[chloro(methyl)phosphoryl]ethane Chemical compound CCP(C)(Cl)=O KJKWGCTWYJCDHP-UHFFFAOYSA-N 0.000 description 1
- SMDZCTRRPHMTSJ-UHFFFAOYSA-N 3-[chloro(ethyl)phosphoryl]-2-methylpropanoyl chloride Chemical compound CCP(Cl)(=O)CC(C)C(Cl)=O SMDZCTRRPHMTSJ-UHFFFAOYSA-N 0.000 description 1
- GRNZQINGIYXHDA-UHFFFAOYSA-N 3-[chloro(ethyl)phosphoryl]propanoyl chloride Chemical compound CCP(Cl)(=O)CCC(Cl)=O GRNZQINGIYXHDA-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- LWNLXVXSCCLRRZ-UHFFFAOYSA-N dichlorophosphane Chemical compound ClPCl LWNLXVXSCCLRRZ-UHFFFAOYSA-N 0.000 description 1
- 239000012757 flame retardant agent Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/34—Halides thereof
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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752529731 DE2529731C2 (de) | 1975-07-03 | Verfahren zur Herstellung von [beta-(Halogenformyl) äthyl] -phosphinsäurehalogeniden |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE43253L IE43253L (en) | 1977-01-03 |
| IE43253B1 true IE43253B1 (en) | 1981-01-14 |
Family
ID=5950600
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE1458/76A IE43253B1 (en) | 1975-07-03 | 1976-07-02 | Production of beta-halogenformyl-ethyl phosphinic acid halides |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4022826A (enExample) |
| JP (1) | JPS527926A (enExample) |
| AT (1) | AT339921B (enExample) |
| BE (1) | BE843601A (enExample) |
| CA (1) | CA1060469A (enExample) |
| CH (1) | CH619963A5 (enExample) |
| DD (1) | DD124987A5 (enExample) |
| FR (1) | FR2316243A1 (enExample) |
| GB (1) | GB1494610A (enExample) |
| IE (1) | IE43253B1 (enExample) |
| IT (1) | IT1063628B (enExample) |
| NL (1) | NL182078C (enExample) |
| SU (1) | SU676168A3 (enExample) |
| ZA (1) | ZA763944B (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2936609A1 (de) * | 1979-09-11 | 1981-04-02 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von 2-chlorformylethyl-methyl-phosphinsaeurechloriden |
| JPS6159893U (enExample) * | 1984-09-27 | 1986-04-22 | ||
| JP2990953B2 (ja) * | 1991-08-09 | 1999-12-13 | 堺化学工業株式会社 | ホスフィニルカルボン酸誘導体の製造方法 |
| US5374707A (en) * | 1993-02-18 | 1994-12-20 | Monsanto Company | Hydroxy ethyl bibenzoate |
| US5399429A (en) * | 1994-03-11 | 1995-03-21 | Monsanto Company | Flame retardant recycled polyester copolymers |
| US5399428A (en) * | 1994-03-11 | 1995-03-21 | Monsanto Company | Flame retardant polyester copolymers |
| US6797754B2 (en) * | 2002-05-06 | 2004-09-28 | Cheil Industries Inc. | Flame retardant styrenic compositions containing oxaphospholane compound as flame retardant |
| US6838497B2 (en) * | 1998-09-02 | 2005-01-04 | Cheil Industries Inc. | Flame retardant thermoplastic resin composition containing styrene polymer as compatabilizer and oxaphospholane compound as flame retardant |
| DE10153780C1 (de) * | 2001-11-02 | 2002-11-28 | Clariant Gmbh | Verfahren zur Herstellung von Carboxyethylmethylphosphinsäureglykolester und ihre Verwendung |
| US6920827B2 (en) * | 2003-10-31 | 2005-07-26 | Raytheon Company | Vehicle-borne system and method for countering an incoming threat |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH173763A (de) * | 1934-06-04 | 1934-12-15 | Bigler Spichiger & Co A G | Stafetten-Sichtkartei. |
-
1976
- 1976-06-21 IT IT50028/76A patent/IT1063628B/it active
- 1976-06-23 CH CH804976A patent/CH619963A5/de not_active IP Right Cessation
- 1976-06-28 SU SU762377453A patent/SU676168A3/ru active
- 1976-06-29 GB GB26997/76A patent/GB1494610A/en not_active Expired
- 1976-06-29 US US05/700,769 patent/US4022826A/en not_active Expired - Lifetime
- 1976-06-30 DD DD193656A patent/DD124987A5/xx not_active IP Right Cessation
- 1976-06-30 BE BE168476A patent/BE843601A/xx not_active IP Right Cessation
- 1976-07-01 AT AT482176A patent/AT339921B/de not_active IP Right Cessation
- 1976-07-02 ZA ZA763944A patent/ZA763944B/xx unknown
- 1976-07-02 NL NLAANVRAGE7607339,A patent/NL182078C/xx not_active IP Right Cessation
- 1976-07-02 CA CA256,174A patent/CA1060469A/en not_active Expired
- 1976-07-02 JP JP51078823A patent/JPS527926A/ja active Granted
- 1976-07-02 IE IE1458/76A patent/IE43253B1/en unknown
- 1976-07-02 FR FR7620334A patent/FR2316243A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| CH619963A5 (enExample) | 1980-10-31 |
| US4022826A (en) | 1977-05-10 |
| FR2316243A1 (fr) | 1977-01-28 |
| ATA482176A (de) | 1977-03-15 |
| IT1063628B (it) | 1985-02-11 |
| JPS527926A (en) | 1977-01-21 |
| ZA763944B (en) | 1977-06-29 |
| NL182078B (nl) | 1987-08-03 |
| AT339921B (de) | 1977-11-10 |
| GB1494610A (en) | 1977-12-07 |
| DD124987A5 (enExample) | 1977-03-23 |
| DE2529731B1 (de) | 1976-12-02 |
| BE843601A (fr) | 1976-12-30 |
| CA1060469A (en) | 1979-08-14 |
| DE2529731A1 (enExample) | 1976-12-02 |
| IE43253L (en) | 1977-01-03 |
| JPS5516516B2 (enExample) | 1980-05-02 |
| FR2316243B1 (enExample) | 1979-08-17 |
| NL182078C (nl) | 1988-01-04 |
| SU676168A3 (ru) | 1979-07-25 |
| NL7607339A (nl) | 1977-01-05 |
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