CA1126482A - Reactifs de grignard et leur procede de preparation - Google Patents
Reactifs de grignard et leur procede de preparationInfo
- Publication number
- CA1126482A CA1126482A CA290,395A CA290395A CA1126482A CA 1126482 A CA1126482 A CA 1126482A CA 290395 A CA290395 A CA 290395A CA 1126482 A CA1126482 A CA 1126482A
- Authority
- CA
- Canada
- Prior art keywords
- reaction
- metal
- charac
- magnesium
- terized
- 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.)
- Expired
Links
- 238000000034 method Methods 0.000 title claims description 34
- 230000008569 process Effects 0.000 title claims description 17
- 238000002360 preparation method Methods 0.000 title abstract description 5
- 150000004795 grignard reagents Chemical class 0.000 title description 7
- 239000011777 magnesium Substances 0.000 claims abstract description 28
- 229910052751 metal Inorganic materials 0.000 claims abstract description 27
- 239000002184 metal Substances 0.000 claims abstract description 27
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 21
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 19
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 19
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 19
- -1 organometallic halides Chemical class 0.000 claims abstract description 15
- 239000002904 solvent Substances 0.000 claims abstract description 15
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 13
- 229910052790 beryllium Inorganic materials 0.000 claims abstract description 7
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 claims abstract description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 6
- 239000011701 zinc Substances 0.000 claims abstract description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 5
- 239000011575 calcium Substances 0.000 claims abstract description 5
- 238000006243 chemical reaction Methods 0.000 claims description 53
- 239000007789 gas Substances 0.000 claims description 15
- 150000004820 halides Chemical class 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000003153 chemical reaction reagent Substances 0.000 claims description 11
- 150000002367 halogens Chemical group 0.000 claims description 11
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 7
- 229930195733 hydrocarbon Natural products 0.000 claims description 7
- 238000009835 boiling Methods 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 4
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 4
- 150000002739 metals Chemical class 0.000 claims description 4
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 239000012190 activator Substances 0.000 claims description 3
- 238000000354 decomposition reaction Methods 0.000 claims description 3
- 125000002524 organometallic group Chemical group 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 238000000137 annealing Methods 0.000 claims description 2
- 239000012298 atmosphere Substances 0.000 claims description 2
- GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 claims description 2
- 238000010924 continuous production Methods 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 230000009467 reduction Effects 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 239000000725 suspension Substances 0.000 claims description 2
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 239000012535 impurity Substances 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 abstract description 4
- 229910001507 metal halide Inorganic materials 0.000 abstract description 2
- 150000005309 metal halides Chemical class 0.000 abstract description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- 239000000843 powder Substances 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 238000004458 analytical method Methods 0.000 description 9
- 235000013350 formula milk Nutrition 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- 229910012375 magnesium hydride Inorganic materials 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 150000002894 organic compounds Chemical class 0.000 description 5
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000007818 Grignard reagent Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 229940058494 beryllium Drugs 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- 150000002901 organomagnesium compounds Chemical class 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 238000001632 acidimetric titration Methods 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000004703 alkoxides Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910000039 hydrogen halide Inorganic materials 0.000 description 2
- 239000012433 hydrogen halide Substances 0.000 description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- OTCKOJUMXQWKQG-UHFFFAOYSA-L magnesium bromide Chemical compound [Mg+2].[Br-].[Br-] OTCKOJUMXQWKQG-UHFFFAOYSA-L 0.000 description 2
- 229910001623 magnesium bromide Inorganic materials 0.000 description 2
- QUXHCILOWRXCEO-UHFFFAOYSA-M magnesium;butane;chloride Chemical compound [Mg+2].[Cl-].CCC[CH2-] QUXHCILOWRXCEO-UHFFFAOYSA-M 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 238000000197 pyrolysis Methods 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- 229930003347 Atropine Natural products 0.000 description 1
- 229910014265 BrCl Inorganic materials 0.000 description 1
- PZOJUJCALDFFHC-UHFFFAOYSA-M Br[Mg]C1CCCC1 Chemical compound Br[Mg]C1CCCC1 PZOJUJCALDFFHC-UHFFFAOYSA-M 0.000 description 1
- 101100298222 Caenorhabditis elegans pot-1 gene Proteins 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical class [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- UCVIZTDOJLBADJ-UHFFFAOYSA-M Cl[Mg]C1C=CC=C1 Chemical compound Cl[Mg]C1C=CC=C1 UCVIZTDOJLBADJ-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000003747 Grignard reaction Methods 0.000 description 1
- 241000243251 Hydra Species 0.000 description 1
- RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 101100166829 Mus musculus Cenpk gene Proteins 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000212342 Sium Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000004171 alkoxy aryl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- RKUNBYITZUJHSG-SPUOUPEWSA-N atropine Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-SPUOUPEWSA-N 0.000 description 1
- 229960000396 atropine Drugs 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- CODNYICXDISAEA-UHFFFAOYSA-N bromine monochloride Chemical compound BrCl CODNYICXDISAEA-UHFFFAOYSA-N 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- QILSFLSDHQAZET-UHFFFAOYSA-N diphenylmethanol Chemical compound C=1C=CC=CC=1C(O)C1=CC=CC=C1 QILSFLSDHQAZET-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 229960002089 ferrous chloride Drugs 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- BLQJIBCZHWBKSL-UHFFFAOYSA-L magnesium iodide Chemical compound [Mg+2].[I-].[I-] BLQJIBCZHWBKSL-UHFFFAOYSA-L 0.000 description 1
- 229910001641 magnesium iodide Inorganic materials 0.000 description 1
- NIXOIRLDFIPNLJ-UHFFFAOYSA-M magnesium;benzene;bromide Chemical compound [Mg+2].[Br-].C1=CC=[C-]C=C1 NIXOIRLDFIPNLJ-UHFFFAOYSA-M 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- RXQCGGRTAILOIN-UHFFFAOYSA-N mephentermine Chemical compound CNC(C)(C)CC1=CC=CC=C1 RXQCGGRTAILOIN-UHFFFAOYSA-N 0.000 description 1
- 229960002342 mephentermine Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000002911 mydriatic effect Effects 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000002734 organomagnesium group Chemical group 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 235000020610 powder formula Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F5/00—Compounds of magnesium
- C01F5/26—Magnesium halides
- C01F5/30—Chlorides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/02—Halides of titanium
-
- 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
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
-
- 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
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
- C07F3/02—Magnesium compounds
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Geology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Glass Compositions (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000400359A CA1145530A (fr) | 1976-11-09 | 1982-04-01 | Reactifs de grignard et leur procede de preparation |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7633757A FR2370054A1 (fr) | 1976-11-09 | 1976-11-09 | Reactifs de grignard, leur procede de preparation et leur application a la synthese d'halogenure de magnesium anhydre |
| FR76/33.757 | 1976-11-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1126482A true CA1126482A (fr) | 1982-06-29 |
Family
ID=9179700
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA290,395A Expired CA1126482A (fr) | 1976-11-09 | 1977-11-08 | Reactifs de grignard et leur procede de preparation |
Country Status (16)
| Country | Link |
|---|---|
| US (3) | US4187254A (enExample) |
| JP (1) | JPS5359628A (enExample) |
| AU (1) | AU521017B2 (enExample) |
| BE (1) | BE860580A (enExample) |
| BR (1) | BR7707472A (enExample) |
| CA (1) | CA1126482A (enExample) |
| CH (2) | CH629213A5 (enExample) |
| DE (1) | DE2749983A1 (enExample) |
| ES (2) | ES473049A1 (enExample) |
| FR (1) | FR2370054A1 (enExample) |
| GB (1) | GB1561730A (enExample) |
| IN (2) | IN147281B (enExample) |
| IT (1) | IT1091035B (enExample) |
| NL (1) | NL7712360A (enExample) |
| NO (4) | NO773824L (enExample) |
| TR (1) | TR20857A (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2370054A1 (fr) * | 1976-11-09 | 1978-06-02 | Charbonnages Ste Chimique | Reactifs de grignard, leur procede de preparation et leur application a la synthese d'halogenure de magnesium anhydre |
| FR2424760A1 (fr) * | 1978-05-05 | 1979-11-30 | Charbonnages Ste Chimique | Catalyseurs comprenant du magnesium et un metal de transition |
| FR2464922A1 (fr) * | 1979-09-13 | 1981-03-20 | Charbonnages Ste Chimique | Procede de reduction d'halogenures metalliques en phase vapeur par des composes organomagnesiens solides et produits reduits obtenus |
| DE3244972C1 (de) * | 1982-12-04 | 1984-02-09 | Condea Chemie GmbH, 2212 Brunsbüttel | Verfahren und Vorrichtung zur kontinuierlichen Herstellung von Aluminiumalkoholaten |
| US4764347A (en) * | 1983-04-05 | 1988-08-16 | Milligan John D | Grid plate assembly for ebullated bed reactor |
| DE3722993A1 (de) * | 1987-07-11 | 1989-01-19 | Studiengesellschaft Kohle Mbh | Loesliche magnesiumdihydride, verfahren zu ihrer herstellung und ihre verwendung |
| GB9126339D0 (en) * | 1991-12-11 | 1992-02-12 | Ici Plc | Chemical process |
| US6395840B1 (en) * | 1997-10-03 | 2002-05-28 | Southwest Research Institute | Precursor polymers to refractory metal carbides and metal borides |
| DE19757499A1 (de) * | 1997-12-23 | 1999-06-24 | Studiengesellschaft Kohle Mbh | Verfahren zur Synthese von Organomagnesium-Verbindungen unter Einsatz von Katalysatoren |
| CN102093396B (zh) * | 2010-12-27 | 2012-07-25 | 浙江新和成股份有限公司 | 一种格氏试剂的制备方法 |
| US9815918B2 (en) | 2012-03-19 | 2017-11-14 | Formosa Plastics Corporation, U.S.A. | Catalyst component for high activity and high stereoselectivity in olefin polymerization |
| WO2021056193A1 (zh) * | 2019-09-24 | 2021-04-01 | 凯莱英医药集团（天津）股份有限公司 | 一种苄基卤化锌及其衍生物的连续制备方法 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1992090A (en) * | 1930-12-22 | 1935-02-19 | Pestalozza Paolo | Process for mixing gases and solids |
| US2066198A (en) * | 1932-02-26 | 1936-12-29 | Standard Oil Dev Co | Process for preparing grignard compounds |
| US2464685A (en) * | 1946-12-02 | 1949-03-15 | Diamond Alkali Co | Continuous grignard method |
| DE847595C (de) * | 1951-03-17 | 1952-08-25 | Richard Dipl-Chem Bauer | Verfahren zur Herstellung von Grignardverbindungen |
| US2852544A (en) * | 1955-10-26 | 1958-09-16 | Phillips Petroleum Co | Preparation of organometallic halides |
| GB955806A (en) * | 1959-04-29 | 1964-04-22 | Nat Res Dev | Preparation and use of organomagnesium materials |
| US3144473A (en) * | 1959-08-17 | 1964-08-11 | Shell Oil Co | Method for preparing zinc dialkyls suitable for use in polymerization catalysts |
| US3140321A (en) * | 1960-02-16 | 1964-07-07 | Cincinnati Milling Machine Co | Preparation of grignard reagents in predominantly hydrocarbon media |
| US3137714A (en) * | 1960-10-27 | 1964-06-16 | Exxon Research Engineering Co | Preparation of organomercurials |
| US3095460A (en) * | 1961-10-25 | 1963-06-25 | Dow Chemical Co | Preparation of stabilized magnesium alkyls |
| GB1051394A (enExample) * | 1964-10-06 | |||
| NL162921B (nl) * | 1969-01-10 | 1980-02-15 | Montedison Spa | Werkwijze om een katalysator te bereiden voor de polymerisatie van alkenen-1. |
| US3641081A (en) * | 1969-01-21 | 1972-02-08 | Int Lead Zinc Res | Process for preparing dialkylzinc compounds from alkylbromide |
| US3766280A (en) * | 1970-10-28 | 1973-10-16 | Lithium Corp | Diorganomagnesium reagents and methods of preparing same |
| US3755478A (en) * | 1971-08-18 | 1973-08-28 | Lithium Corp | Cyclic process for the preparation of diorganomagnesium compounds |
| FR2370054A1 (fr) * | 1976-11-09 | 1978-06-02 | Charbonnages Ste Chimique | Reactifs de grignard, leur procede de preparation et leur application a la synthese d'halogenure de magnesium anhydre |
| FR2424760A1 (fr) * | 1978-05-05 | 1979-11-30 | Charbonnages Ste Chimique | Catalyseurs comprenant du magnesium et un metal de transition |
| FR2464922A1 (fr) * | 1979-09-13 | 1981-03-20 | Charbonnages Ste Chimique | Procede de reduction d'halogenures metalliques en phase vapeur par des composes organomagnesiens solides et produits reduits obtenus |
| SU1449139A1 (ru) * | 1986-01-21 | 1989-01-07 | Ставропольский государственный педагогический институт | Акробатическа дорожка |
-
1976
- 1976-11-09 FR FR7633757A patent/FR2370054A1/fr active Granted
- 1976-11-09 ES ES473049A patent/ES473049A1/es not_active Expired
-
1977
- 1977-03-03 IN IN370/DEL/77A patent/IN147281B/en unknown
- 1977-10-21 CH CH1282777A patent/CH629213A5/fr not_active IP Right Cessation
- 1977-11-02 US US05/847,824 patent/US4187254A/en not_active Expired - Lifetime
- 1977-11-03 AU AU30277/77A patent/AU521017B2/en not_active Expired
- 1977-11-07 GB GB46175/77A patent/GB1561730A/en not_active Expired
- 1977-11-08 CA CA290,395A patent/CA1126482A/fr not_active Expired
- 1977-11-08 BR BR7707472A patent/BR7707472A/pt unknown
- 1977-11-08 NO NO773824A patent/NO773824L/no unknown
- 1977-11-08 BE BE2056414A patent/BE860580A/xx not_active IP Right Cessation
- 1977-11-08 IT IT69502/77A patent/IT1091035B/it active
- 1977-11-08 DE DE19772749983 patent/DE2749983A1/de not_active Withdrawn
- 1977-11-09 TR TR20857A patent/TR20857A/xx unknown
- 1977-11-09 JP JP13518377A patent/JPS5359628A/ja active Pending
- 1977-11-09 NL NL7712360A patent/NL7712360A/xx not_active Application Discontinuation
- 1977-11-10 ES ES464010A patent/ES464010A1/es not_active Expired
-
1979
- 1979-11-21 IN IN839/DEL/79A patent/IN149351B/en unknown
-
1981
- 1981-03-30 US US06/249,206 patent/US4366140A/en not_active Expired - Fee Related
- 1981-07-30 CH CH494081A patent/CH628903A5/fr not_active IP Right Cessation
-
1982
- 1982-09-22 US US06/421,499 patent/US4474703A/en not_active Expired - Fee Related
- 1982-10-08 NO NO823382A patent/NO823382L/no unknown
- 1982-10-08 NO NO823381A patent/NO823381L/no unknown
-
1984
- 1984-02-13 NO NO840514A patent/NO840514L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NO823382L (no) | 1978-05-10 |
| IN149351B (enExample) | 1981-10-31 |
| JPS5359628A (en) | 1978-05-29 |
| NL7712360A (nl) | 1978-05-11 |
| AU3027777A (en) | 1979-05-10 |
| GB1561730A (en) | 1980-02-27 |
| ES473049A1 (es) | 1979-10-16 |
| US4366140A (en) | 1982-12-28 |
| CH629213A5 (fr) | 1982-04-15 |
| TR20857A (tr) | 1982-11-01 |
| IN147281B (enExample) | 1980-01-19 |
| NO840514L (no) | 1978-05-10 |
| CH628903A5 (fr) | 1982-03-31 |
| NO773824L (no) | 1978-05-10 |
| FR2370054B1 (enExample) | 1980-11-07 |
| AU521017B2 (en) | 1982-03-11 |
| ES464010A1 (es) | 1978-11-16 |
| DE2749983A1 (de) | 1978-05-11 |
| US4474703A (en) | 1984-10-02 |
| BR7707472A (pt) | 1978-06-20 |
| US4187254A (en) | 1980-02-05 |
| FR2370054A1 (fr) | 1978-06-02 |
| BE860580A (fr) | 1978-05-08 |
| IT1091035B (it) | 1985-06-26 |
| NO823381L (no) | 1978-05-10 |
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