CH615438A5 - - Google Patents
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- Publication number
- CH615438A5 CH615438A5 CH327977A CH327977A CH615438A5 CH 615438 A5 CH615438 A5 CH 615438A5 CH 327977 A CH327977 A CH 327977A CH 327977 A CH327977 A CH 327977A CH 615438 A5 CH615438 A5 CH 615438A5
- Authority
- CH
- Switzerland
- Prior art keywords
- carbon atoms
- group
- formula
- alkyl
- reaction
- Prior art date
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 23
- 239000002253 acid Substances 0.000 claims description 18
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 17
- 238000006243 chemical reaction Methods 0.000 claims description 16
- -1 phenyl - Chemical class 0.000 claims 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 description 15
- 150000001875 compounds Chemical class 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 7
- 239000011541 reaction mixture Substances 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 229910000039 hydrogen halide Inorganic materials 0.000 claims description 5
- 239000012433 hydrogen halide Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 239000012442 inert solvent Substances 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Chemical group 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 238000004821 distillation Methods 0.000 claims description 2
- 238000000605 extraction Methods 0.000 claims description 2
- 239000011261 inert gas Substances 0.000 claims description 2
- 239000000376 reactant Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims 7
- 150000002367 halogens Chemical group 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 238000002360 preparation method Methods 0.000 claims 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims 2
- 238000006467 substitution reaction Methods 0.000 claims 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
- 229920002554 vinyl polymer Polymers 0.000 claims 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 239000006227 byproduct Substances 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000002843 carboxylic acid group Chemical group 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 150000004820 halides Chemical class 0.000 description 14
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 13
- INUNLMUAPJVRME-UHFFFAOYSA-N 3-chloropropanoyl chloride Chemical compound ClCCC(Cl)=O INUNLMUAPJVRME-UHFFFAOYSA-N 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 6
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 5
- LFMAOMQWCSTELR-UHFFFAOYSA-N 2-methyl-2-oxo-1,2$l^{5}-oxaphospholan-5-one Chemical compound CP1(=O)CCC(=O)O1 LFMAOMQWCSTELR-UHFFFAOYSA-N 0.000 description 4
- CDPKWOKGVUHZFR-UHFFFAOYSA-N dichloro(methyl)phosphane Chemical compound CP(Cl)Cl CDPKWOKGVUHZFR-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 238000005292 vacuum distillation Methods 0.000 description 3
- SGGKZWABPPXBNE-UHFFFAOYSA-N 3-[chloro(methyl)phosphoryl]propanoyl chloride Chemical compound CP(Cl)(=O)CCC(Cl)=O SGGKZWABPPXBNE-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 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 1
- DXWHKNNXPBCIBK-UHFFFAOYSA-N 2,3-dimethyl-2-oxo-1,2lambda5-oxaphospholan-5-one Chemical compound CP1(OC(CC1C)=O)=O DXWHKNNXPBCIBK-UHFFFAOYSA-N 0.000 description 1
- 125000000143 2-carboxyethyl group Chemical group [H]OC(=O)C([H])([H])C([H])([H])* 0.000 description 1
- ZRMHFHDBFAOCKY-UHFFFAOYSA-N 3-[anthracen-1-yl(chloro)phosphoryl]propanoyl chloride Chemical compound C1=CC=C2C=C3C(P(Cl)(=O)CCC(=O)Cl)=CC=CC3=CC2=C1 ZRMHFHDBFAOCKY-UHFFFAOYSA-N 0.000 description 1
- VEMLGDXPZVEULJ-UHFFFAOYSA-N 3-[benzyl(chloro)phosphoryl]propanoyl chloride Chemical compound ClC(=O)CCP(Cl)(=O)CC1=CC=CC=C1 VEMLGDXPZVEULJ-UHFFFAOYSA-N 0.000 description 1
- FLJSBKGKYSDECE-UHFFFAOYSA-N 3-[butyl(chloro)phosphoryl]propanoyl chloride Chemical compound CCCCP(Cl)(=O)CCC(Cl)=O FLJSBKGKYSDECE-UHFFFAOYSA-N 0.000 description 1
- MVYVROMUJVPMMM-UHFFFAOYSA-N 3-[chloro(3-chloropropyl)phosphoryl]propanoyl chloride Chemical compound ClCCCP(Cl)(=O)CCC(Cl)=O MVYVROMUJVPMMM-UHFFFAOYSA-N 0.000 description 1
- DIJAVRIDVIBZRR-UHFFFAOYSA-N 3-[chloro(chloromethyl)phosphoryl]propanoyl chloride Chemical compound ClCP(Cl)(=O)CCC(Cl)=O DIJAVRIDVIBZRR-UHFFFAOYSA-N 0.000 description 1
- KRSWUYQFXVVLLQ-UHFFFAOYSA-N 3-[chloro(cyclohexyl)phosphoryl]propanoyl chloride Chemical compound ClC(=O)CCP(Cl)(=O)C1CCCCC1 KRSWUYQFXVVLLQ-UHFFFAOYSA-N 0.000 description 1
- AJPZPSNPNWIYNM-UHFFFAOYSA-N 3-[chloro(cyclooctyl)phosphoryl]propanoyl chloride Chemical compound ClC(=O)CCP(Cl)(=O)C1CCCCCCC1 AJPZPSNPNWIYNM-UHFFFAOYSA-N 0.000 description 1
- WKWSPDBCXKUWRB-UHFFFAOYSA-N 3-[chloro(dodecyl)phosphoryl]propanoyl chloride Chemical compound CCCCCCCCCCCCP(Cl)(=O)CCC(Cl)=O WKWSPDBCXKUWRB-UHFFFAOYSA-N 0.000 description 1
- QNCDNZDZAIPYFT-UHFFFAOYSA-N 3-[chloro(ethenyl)phosphoryl]propanoyl chloride Chemical compound ClC(=O)CCP(Cl)(=O)C=C QNCDNZDZAIPYFT-UHFFFAOYSA-N 0.000 description 1
- CKOVISHJAJMUNY-UHFFFAOYSA-N 3-[chloro(hexadecyl)phosphoryl]propanoyl chloride Chemical compound CCCCCCCCCCCCCCCCP(Cl)(=O)CCC(Cl)=O CKOVISHJAJMUNY-UHFFFAOYSA-N 0.000 description 1
- GISHPKOGHPXFBJ-UHFFFAOYSA-N 3-[chloro(methyl)phosphoryl]butanoyl chloride Chemical compound CP(=O)(Cl)C(C)CC(Cl)=O GISHPKOGHPXFBJ-UHFFFAOYSA-N 0.000 description 1
- UPSVZRZOPHRLGQ-UHFFFAOYSA-N 3-[chloro(naphthalen-1-yl)phosphoryl]propanoyl chloride Chemical compound C1=CC=C2C(P(Cl)(=O)CCC(=O)Cl)=CC=CC2=C1 UPSVZRZOPHRLGQ-UHFFFAOYSA-N 0.000 description 1
- CZUDUOCOKAJRLA-UHFFFAOYSA-N 3-[chloro(oct-1-enyl)phosphoryl]propanoyl chloride Chemical compound ClC(=O)CCP(=O)(C=CCCCCCC)Cl CZUDUOCOKAJRLA-UHFFFAOYSA-N 0.000 description 1
- YTMPIQPLZHJTPK-UHFFFAOYSA-N 3-[chloro(octadecyl)phosphoryl]propanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCCP(Cl)(=O)CCC(Cl)=O YTMPIQPLZHJTPK-UHFFFAOYSA-N 0.000 description 1
- UJAOINCKNUZPQC-UHFFFAOYSA-N 3-[chloro(octyl)phosphoryl]propanoyl chloride Chemical compound CCCCCCCCP(Cl)(=O)CCC(Cl)=O UJAOINCKNUZPQC-UHFFFAOYSA-N 0.000 description 1
- 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 1
- DXKABWRFHUTSMM-UHFFFAOYSA-N 3-[chloro(prop-1-enyl)phosphoryl]propanoyl chloride Chemical compound CC=CP(Cl)(=O)CCC(Cl)=O DXKABWRFHUTSMM-UHFFFAOYSA-N 0.000 description 1
- CJEFGSMAERCPJC-UHFFFAOYSA-N 3-[chloro(propyl)phosphoryl]propanoyl chloride Chemical compound CCCP(Cl)(=O)CCC(Cl)=O CJEFGSMAERCPJC-UHFFFAOYSA-N 0.000 description 1
- KEFHFGJDPLCNII-UHFFFAOYSA-N 3-[chloro-(4-chlorophenyl)phosphoryl]propanoyl chloride Chemical compound ClC(=O)CCP(Cl)(=O)C1=CC=C(Cl)C=C1 KEFHFGJDPLCNII-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- VMEOAIGRDIYFQS-UHFFFAOYSA-N ClC(=O)CCP(=O)Cl Chemical compound ClC(=O)CCP(=O)Cl VMEOAIGRDIYFQS-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- SSHDEAQDXLFSAF-UHFFFAOYSA-N O=C1CCP(=O)O1 Chemical class O=C1CCP(=O)O1 SSHDEAQDXLFSAF-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- JDOXUXDGEFQQII-UHFFFAOYSA-N benzyl(dichloro)phosphane Chemical compound ClP(Cl)CC1=CC=CC=C1 JDOXUXDGEFQQII-UHFFFAOYSA-N 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- IKNPUBSFLQLSLS-UHFFFAOYSA-N butyl(dichloro)phosphane Chemical compound CCCCP(Cl)Cl IKNPUBSFLQLSLS-UHFFFAOYSA-N 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- JLUMKVGIQTWWKK-UHFFFAOYSA-N dichloro(chloromethyl)phosphane Chemical compound ClCP(Cl)Cl JLUMKVGIQTWWKK-UHFFFAOYSA-N 0.000 description 1
- MJEQIIGWDHUZJW-UHFFFAOYSA-N dichloro(cyclohexyl)phosphane Chemical compound ClP(Cl)C1CCCCC1 MJEQIIGWDHUZJW-UHFFFAOYSA-N 0.000 description 1
- PVNZKNQSKGENAP-UHFFFAOYSA-N dichloro(dodecyl)phosphane Chemical compound CCCCCCCCCCCCP(Cl)Cl PVNZKNQSKGENAP-UHFFFAOYSA-N 0.000 description 1
- ZMQFCCAWWXHOFA-UHFFFAOYSA-N dichloro(ethenyl)phosphane Chemical compound ClP(Cl)C=C ZMQFCCAWWXHOFA-UHFFFAOYSA-N 0.000 description 1
- JHNJGLVSPIMBLD-UHFFFAOYSA-N dichloro(ethyl)phosphane Chemical compound CCP(Cl)Cl JHNJGLVSPIMBLD-UHFFFAOYSA-N 0.000 description 1
- PVTHAGJZMANMRT-UHFFFAOYSA-N dichloro(propyl)phosphane Chemical compound CCCP(Cl)Cl PVTHAGJZMANMRT-UHFFFAOYSA-N 0.000 description 1
- XAYGGTDUZQMQAR-UHFFFAOYSA-N dichloro-(2-phenylphenyl)phosphane Chemical compound ClP(Cl)C1=CC=CC=C1C1=CC=CC=C1 XAYGGTDUZQMQAR-UHFFFAOYSA-N 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 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
- C07F9/547—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
- C07F9/657163—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 the ring phosphorus atom being bound to at least one carbon atom
- C07F9/657172—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 the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and one oxygen atom being part of a (thio)phosphinic acid ester: (X = O, S)
-
- 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)]
- C07F9/32—Esters thereof
- C07F9/3205—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/3211—Esters of acyclic saturated acids which can have further substituents on alkyl
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762611694 DE2611694A1 (de) | 1976-03-19 | 1976-03-19 | Verfahren zur gleichzeitigen herstellung von 2,5-dioxo-1,2-oxa-phospholanen und beta-halogenpropionsaeurehalogenid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH615438A5 true CH615438A5 (fr) | 1980-01-31 |
Family
ID=5972942
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH327977A CH615438A5 (fr) | 1976-03-19 | 1977-03-16 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4096182A (fr) |
| JP (1) | JPS52113918A (fr) |
| BE (1) | BE852700R (fr) |
| CA (1) | CA1086765A (fr) |
| CH (1) | CH615438A5 (fr) |
| DE (1) | DE2611694A1 (fr) |
| FR (1) | FR2344564A2 (fr) |
| GB (1) | GB1565295A (fr) |
| IT (1) | IT1114767B (fr) |
| NL (1) | NL7702727A (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| EP3502089B1 (fr) | 2017-12-20 | 2020-08-19 | 3M Innovative Properties Company | Procédé de fabrication d'un halogénure de 3-halopropionyle dans un réacteur à écoulement |
| EP3502090B1 (fr) | 2017-12-20 | 2020-08-19 | 3M Innovative Properties Company | Procédé de préparation d'un composé comprenant un groupe (méth) acryloyle |
| CN108373485A (zh) * | 2018-02-27 | 2018-08-07 | 利尔化学股份有限公司 | 一种环状膦酸酐的生产方法及装置 |
| CN114195826B (zh) * | 2021-09-13 | 2023-06-23 | 洪湖市一泰科技有限公司 | 一种环膦酸酐生产中的蒸馏釜残留物的处理方法及处理装置 |
-
1976
- 1976-03-19 DE DE19762611694 patent/DE2611694A1/de not_active Withdrawn
-
1977
- 1977-03-14 NL NL7702727A patent/NL7702727A/xx not_active Application Discontinuation
- 1977-03-16 US US05/778,052 patent/US4096182A/en not_active Expired - Lifetime
- 1977-03-16 CH CH327977A patent/CH615438A5/de not_active IP Right Cessation
- 1977-03-17 JP JP2872477A patent/JPS52113918A/ja active Pending
- 1977-03-17 GB GB11376/77A patent/GB1565295A/en not_active Expired
- 1977-03-17 IT IT7721378A patent/IT1114767B/it active
- 1977-03-18 CA CA274,323A patent/CA1086765A/fr not_active Expired
- 1977-03-21 BE BE175971A patent/BE852700R/fr active
- 1977-03-21 FR FR7708351A patent/FR2344564A2/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| US4096182A (en) | 1978-06-20 |
| FR2344564B2 (fr) | 1981-08-21 |
| IT1114767B (it) | 1986-01-27 |
| BE852700R (fr) | 1977-09-21 |
| JPS52113918A (en) | 1977-09-24 |
| NL7702727A (nl) | 1977-09-21 |
| FR2344564A2 (fr) | 1977-10-14 |
| CA1086765A (fr) | 1980-09-30 |
| GB1565295A (en) | 1980-04-16 |
| DE2611694A1 (de) | 1977-09-22 |
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