CH640207A5 - Process for the preparation of 2,2-dichloro- and bromocyclopropane compounds - Google Patents
Process for the preparation of 2,2-dichloro- and bromocyclopropane compounds Download PDFInfo
- Publication number
- CH640207A5 CH640207A5 CH507378A CH507378A CH640207A5 CH 640207 A5 CH640207 A5 CH 640207A5 CH 507378 A CH507378 A CH 507378A CH 507378 A CH507378 A CH 507378A CH 640207 A5 CH640207 A5 CH 640207A5
- Authority
- CH
- Switzerland
- Prior art keywords
- mmol
- examples
- yield
- preparation
- aqueous phase
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 17
- 238000002360 preparation method Methods 0.000 title claims description 16
- LKXYJYDRLBPHRS-UHFFFAOYSA-N bromocyclopropane Chemical class BrC1CC1 LKXYJYDRLBPHRS-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 39
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 26
- 239000008346 aqueous phase Substances 0.000 claims description 22
- 238000006243 chemical reaction Methods 0.000 claims description 11
- DIKBFYAXUHHXCS-UHFFFAOYSA-N bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 claims description 10
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 9
- 239000003054 catalyst Substances 0.000 claims description 8
- 229950005228 bromoform Drugs 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 230000003197 catalytic effect Effects 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 241000251730 Chondrichthyes Species 0.000 claims 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000008051 alkyl sulfates Chemical class 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
- 150000002894 organic compounds Chemical class 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 52
- 239000000126 substance Substances 0.000 description 25
- -1 ethylene, propylene, 1-butene Chemical class 0.000 description 16
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 14
- 239000011541 reaction mixture Substances 0.000 description 14
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 13
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 12
- 238000003756 stirring Methods 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 8
- 235000019270 ammonium chloride Nutrition 0.000 description 8
- 239000012074 organic phase Substances 0.000 description 8
- YCOZIPAWZNQLMR-UHFFFAOYSA-N pentadecane Chemical compound CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- HYPABJGVBDSCIT-UPHRSURJSA-N cyclododecene Chemical compound C1CCCCC\C=C/CCCC1 HYPABJGVBDSCIT-UPHRSURJSA-N 0.000 description 6
- QEVYQHFZTXUKJU-UHFFFAOYSA-M methyl-tri(octan-2-yl)azanium;chloride Chemical compound [Cl-].CCCCCCC(C)[N+](C)(C(C)CCCCCC)C(C)CCCCCC QEVYQHFZTXUKJU-UHFFFAOYSA-M 0.000 description 6
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 6
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- KNXISWJTUXKGCI-UHFFFAOYSA-N tert-butyl 3-methylbut-2-enoate Chemical compound CC(C)=CC(=O)OC(C)(C)C KNXISWJTUXKGCI-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- ZOLLIQAKMYWTBR-RYMQXAEESA-N cyclododecatriene Chemical compound C/1C\C=C\CC\C=C/CC\C=C\1 ZOLLIQAKMYWTBR-RYMQXAEESA-N 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 description 4
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000001942 cyclopropanes Chemical class 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 150000004010 onium ions Chemical class 0.000 description 3
- 239000007790 solid phase Substances 0.000 description 3
- 150000003509 tertiary alcohols Chemical class 0.000 description 3
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 2
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical compound CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 2
- FRDAATYAJDYRNW-UHFFFAOYSA-N 3-methyl-3-pentanol Chemical compound CCC(C)(O)CC FRDAATYAJDYRNW-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 2
- 150000001925 cycloalkenes Chemical class 0.000 description 2
- DDTBPAQBQHZRDW-UHFFFAOYSA-N cyclododecane Chemical compound C1CCCCCCCCCCC1 DDTBPAQBQHZRDW-UHFFFAOYSA-N 0.000 description 2
- CTRVMZJBEVWFHM-UHFFFAOYSA-N cyclotetradecene Chemical compound C1CCCCCCC=CCCCCC1 CTRVMZJBEVWFHM-UHFFFAOYSA-N 0.000 description 2
- CTRVMZJBEVWFHM-OWOJBTEDSA-N cyclotetradecene Chemical compound C1CCCCCC\C=C\CCCCC1 CTRVMZJBEVWFHM-OWOJBTEDSA-N 0.000 description 2
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pentene-2 Natural products CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 150000003457 sulfones Chemical class 0.000 description 2
- LNEFGAYKTMMXDW-UHFFFAOYSA-N tert-butyl 2,2-dichloro-3,3-dimethylcyclopropane-1-carboxylate Chemical compound CC(C)(C)OC(=O)C1C(C)(C)C1(Cl)Cl LNEFGAYKTMMXDW-UHFFFAOYSA-N 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- LKDQWVKWYGOVJW-UHFFFAOYSA-M triethylsulfanium;iodide Chemical compound [I-].CC[S+](CC)CC LKDQWVKWYGOVJW-UHFFFAOYSA-M 0.000 description 2
- FHBJNBBNAAXQKT-XCADPSHZSA-N (1Z,3Z,5Z)-cyclonona-1,3,5-triene Chemical compound C1C\C=C/C=C\C=C/C1 FHBJNBBNAAXQKT-XCADPSHZSA-N 0.000 description 1
- WFLPGXDWMZEHGP-CLFYSBASSA-N (1z)-1-methylcyclooctene Chemical compound C\C1=C\CCCCCC1 WFLPGXDWMZEHGP-CLFYSBASSA-N 0.000 description 1
- WLWFQGXZIDYWQF-UHFFFAOYSA-N (2,2-dichlorocyclopropyl)benzene Chemical compound ClC1(Cl)CC1C1=CC=CC=C1 WLWFQGXZIDYWQF-UHFFFAOYSA-N 0.000 description 1
- NNBWTSXEHTTWMR-UHFFFAOYSA-N 1,1-dichloro-2,2-dimethylcyclopropane Chemical compound CC1(C)CC1(Cl)Cl NNBWTSXEHTTWMR-UHFFFAOYSA-N 0.000 description 1
- LGHSAVSEBATWBX-UHFFFAOYSA-N 1-bromocyclopropane-1-carboxylic acid Chemical class OC(=O)C1(Br)CC1 LGHSAVSEBATWBX-UHFFFAOYSA-N 0.000 description 1
- ZURWAHNLRNTPBL-UHFFFAOYSA-N 13,13-dichlorobicyclo[10.1.0]tridecane Chemical compound C1CCCCCCCCCC2C(Cl)(Cl)C21 ZURWAHNLRNTPBL-UHFFFAOYSA-N 0.000 description 1
- VEQMUQZKBLIXLT-UHFFFAOYSA-N 2,3-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1C(C)C1C(O)=O VEQMUQZKBLIXLT-UHFFFAOYSA-N 0.000 description 1
- MFGOFGRYDNHJTA-UHFFFAOYSA-N 2-amino-1-(2-fluorophenyl)ethanol Chemical compound NCC(O)C1=CC=CC=C1F MFGOFGRYDNHJTA-UHFFFAOYSA-N 0.000 description 1
- ILPBINAXDRFYPL-UHFFFAOYSA-N 2-octene Chemical compound CCCCCC=CC ILPBINAXDRFYPL-UHFFFAOYSA-N 0.000 description 1
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
- RITONZMLZWYPHW-UHFFFAOYSA-N 3-methylhex-1-ene Chemical compound CCCC(C)C=C RITONZMLZWYPHW-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- DOMOSPVLFLKCKL-UHFFFAOYSA-N 9,9-dichloro-8-methylbicyclo[6.1.0]nonane Chemical compound C1CCCCCC2C(Cl)(Cl)C21C DOMOSPVLFLKCKL-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 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 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical class CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
- BTTDZADGGXIQJC-UHFFFAOYSA-M S(=O)(=O)(OCC)[O-].C(C)[S+](C(CCCCCCCCCC)C)C(CCCCCCCCCC)C Chemical compound S(=O)(=O)(OCC)[O-].C(C)[S+](C(CCCCCCCCCC)C)C(CCCCCCCCCC)C BTTDZADGGXIQJC-UHFFFAOYSA-M 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- IZZOKZMGQDMCAE-XQZFLANJSA-N alpha-L-Rhap-(1->2)-[beta-D-GlcpNAc-(1->3)]-alpha-L-Rhap-(1->3)-alpha-L-Rhap-(1->2)-[beta-D-GlcpNAc-(1->3)]-alpha-L-Rhap Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@@H]1[C@H](O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](O)[C@H](C)O[C@H]1O[C@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H]([C@@H](O)[C@H](C)O[C@H]2O)O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)NC(C)=O)O[C@@H](C)[C@@H]1O IZZOKZMGQDMCAE-XQZFLANJSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- YBOZNTGUYASNRA-UHFFFAOYSA-N beta-Methyl-beta-octylen Natural products CCCCCC=C(C)C YBOZNTGUYASNRA-UHFFFAOYSA-N 0.000 description 1
- HUCVOHYBFXVBRW-UHFFFAOYSA-M caesium hydroxide Inorganic materials [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- UCIYGNATMHQYCT-OWOJBTEDSA-N cyclodecene Chemical compound C1CCCC\C=C\CCC1 UCIYGNATMHQYCT-OWOJBTEDSA-N 0.000 description 1
- ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 description 1
- URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 description 1
- 239000004913 cyclooctene Substances 0.000 description 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-M cyclopropanecarboxylate Chemical compound [O-]C(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-M 0.000 description 1
- AVHHUCROZGSCGZ-OWOJBTEDSA-N cyclotridecene Chemical compound C1CCCCC\C=C\CCCCC1 AVHHUCROZGSCGZ-OWOJBTEDSA-N 0.000 description 1
- GMUVJAZTJOCSND-OWOJBTEDSA-N cycloundecene Chemical compound C1CCCC\C=C\CCCC1 GMUVJAZTJOCSND-OWOJBTEDSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- PWLCLNYZHRGZJS-UHFFFAOYSA-M dodecan-2-yl-ethyl-hexadecan-2-ylsulfanium;ethyl sulfate Chemical compound CCOS([O-])(=O)=O.CCCCCCCCCCCCCCC(C)[S+](CC)C(C)CCCCCCCCCC PWLCLNYZHRGZJS-UHFFFAOYSA-M 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000001030 gas--liquid chromatography Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- WZHKDGJSXCTSCK-UHFFFAOYSA-N hept-3-ene Chemical compound CCCC=CCC WZHKDGJSXCTSCK-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NZXZUIRYAWYJHN-UHFFFAOYSA-M hexadecan-2-yl(dimethyl)sulfanium;iodide Chemical compound [I-].CCCCCCCCCCCCCCC(C)[S+](C)C NZXZUIRYAWYJHN-UHFFFAOYSA-M 0.000 description 1
- PKSRDJZZJZNWQB-UHFFFAOYSA-M hexadecyl(dimethyl)sulfanium;methyl sulfate Chemical compound COS([O-])(=O)=O.CCCCCCCCCCCCCCCC[S+](C)C PKSRDJZZJZNWQB-UHFFFAOYSA-M 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- WMFOQBRAJBCJND-UHFFFAOYSA-M lithium hydroxide Inorganic materials [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- MCVVUJPXSBQTRZ-ONEGZZNKSA-N methyl (e)-but-2-enoate Chemical compound COC(=O)\C=C\C MCVVUJPXSBQTRZ-ONEGZZNKSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- QTYFQZHJYYULRV-UHFFFAOYSA-N n-methyloctan-2-amine;hydrochloride Chemical compound Cl.CCCCCCC(C)NC QTYFQZHJYYULRV-UHFFFAOYSA-N 0.000 description 1
- YCBSHDKATAPNIA-UHFFFAOYSA-N non-3-ene Chemical compound CCCCCC=CCC YCBSHDKATAPNIA-UHFFFAOYSA-N 0.000 description 1
- QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- CPRMKOQKXYSDML-UHFFFAOYSA-M rubidium hydroxide Inorganic materials [OH-].[Rb+] CPRMKOQKXYSDML-UHFFFAOYSA-M 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- SNIFAVVHRQZYGO-UHFFFAOYSA-N tetradec-5-ene Chemical compound CCCCCCCCC=CCCCC SNIFAVVHRQZYGO-UHFFFAOYSA-N 0.000 description 1
- GOTIICCWNAPLMN-UHFFFAOYSA-M trimethylsulfanium;bromide Chemical compound [Br-].C[S+](C)C GOTIICCWNAPLMN-UHFFFAOYSA-M 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C67/347—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB19989/77A GB1600414A (en) | 1977-05-12 | 1977-05-12 | Preparation of dihalocyclopropane derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH640207A5 true CH640207A5 (en) | 1983-12-30 |
Family
ID=10138484
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH507378A CH640207A5 (en) | 1977-05-12 | 1978-05-10 | Process for the preparation of 2,2-dichloro- and bromocyclopropane compounds |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS53141246A (enrdf_load_stackoverflow) |
| AU (1) | AU527083B2 (enrdf_load_stackoverflow) |
| CH (1) | CH640207A5 (enrdf_load_stackoverflow) |
| DE (1) | DE2820410A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2390411A1 (enrdf_load_stackoverflow) |
| GB (1) | GB1600414A (enrdf_load_stackoverflow) |
| NL (1) | NL7804900A (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI312795B (en) * | 2002-10-29 | 2009-08-01 | Dai Ichi Kogyo Seiyaku Co Ltd | Flame retardants for plastics |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3265743A (en) * | 1962-05-14 | 1966-08-09 | Ethyl Corp | Production of dihalocarbene adducts |
| US3375286A (en) * | 1965-10-04 | 1968-03-26 | Texaco Inc | Preparation of 1, 1-dichlorocyclopropane compounds |
| GB1323183A (en) * | 1971-01-14 | 1973-07-11 | Bdh Pharmaceuticals Ltd | Cyclopropane esters and acids thereof |
| GB1432540A (en) * | 1972-05-16 | 1976-04-22 | Shell Int Research | Process for the preparation of cyclopropane derivatives |
| US4008287A (en) * | 1972-05-16 | 1977-02-15 | Shell Oil Company | Process for the preparation of cyclopropane derivatives |
| US4012430A (en) * | 1972-05-16 | 1977-03-15 | Shell Oil Company | Process for the preparation of cyclopropane derivatives |
-
1977
- 1977-05-12 GB GB19989/77A patent/GB1600414A/en not_active Expired
-
1978
- 1978-05-08 NL NL7804900A patent/NL7804900A/xx not_active Application Discontinuation
- 1978-05-10 FR FR7813904A patent/FR2390411A1/fr active Granted
- 1978-05-10 JP JP5455978A patent/JPS53141246A/ja active Granted
- 1978-05-10 DE DE19782820410 patent/DE2820410A1/de active Granted
- 1978-05-10 CH CH507378A patent/CH640207A5/de not_active IP Right Cessation
- 1978-05-10 AU AU35988/78A patent/AU527083B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2390411B1 (enrdf_load_stackoverflow) | 1981-01-02 |
| JPS53141246A (en) | 1978-12-08 |
| NL7804900A (nl) | 1978-11-14 |
| JPS6160053B2 (enrdf_load_stackoverflow) | 1986-12-19 |
| AU3598878A (en) | 1979-12-06 |
| GB1600414A (en) | 1981-10-14 |
| AU527083B2 (en) | 1983-02-17 |
| DE2820410C2 (enrdf_load_stackoverflow) | 1987-12-03 |
| DE2820410A1 (de) | 1978-11-16 |
| FR2390411A1 (fr) | 1978-12-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1221224B (de) | Verfahren zur Herstellung von Carbonsaeureestern | |
| DE69914469T2 (de) | Verfahren zur herstellung von hinokitiol | |
| DE2445561C3 (de) | Katalysator zur Umwandlung von Kohlenwasserstoffen und Verwendung desselben | |
| DE2063515A1 (de) | Verfahren zur Herstellung von unge sattigten Carbonsaureestern | |
| DE3152701C2 (de) | Verfahren zur Herstellung von im wesentlichen reinem m-Isopropylphenol | |
| DE2937840C2 (de) | Verfahren zur Herstellung von Diolen, Triolen bzw. Tetrolen durch Hydroxylierung von aliphatischen Mono- oder Diolefinen | |
| DE2820410C2 (enrdf_load_stackoverflow) | ||
| EP0055387B1 (de) | Verfahren zur Herstellung von Epoxiden | |
| DE1804878C3 (de) | Verfahren zur Herstellung von 5-Isopropyliden-2-norbornen durch Isomerisieren von 5-Isopropenyl-2-norbornen | |
| DE69008778T2 (de) | Alkenkupplung. | |
| EP0025940B1 (de) | Verfahren zur Hydroxylierung olefinisch ungesättigter Verbindungen | |
| DE1793385C3 (de) | Verfahren zur Fluorierung von ungesättigten organischen Verbindungen mit einem Hypofluorit | |
| DE1593245A1 (de) | Verfahren zum Herstellen von Cyclododecatrien-(1,5,9) | |
| DE3785032T2 (de) | Carbonsäuregemisch und Verfahren zu seiner Herstellung. | |
| DE2421168C3 (de) | Verfahren zur Herstellung von Cumol und bzw. oder sek.-Butylbenzol | |
| CH626315A5 (en) | Process for preparing aliphatic compounds with olefinic double bonds | |
| DE2551586C2 (de) | Verfahren zur Herstellung von 1,5-Dimethylcycloocten | |
| DE2341240C2 (de) | Verfahren zur Herstellung von Hydroxysulfonen | |
| DD143598A5 (de) | Verfahren zur erniedrigung des 2,6-dialkylphenolgehaltes einer alkylphenolmischung | |
| DE1568763C3 (de) | Verfahren zur gleichzeitigen Herstellung von Isopren und eines Epoxyds oder eines Acrylate oder eines Oxims | |
| CH632730A5 (en) | Process for the preparation of branched olefins | |
| DE1593263C3 (de) | Verfahren zur katalytsichen Umwandlung eines Alkenylcyclohexens und 1,2-Bis-(3'-cyclohexenyl-(1 )-äthylen als solches | |
| DE1668280B2 (de) | Verfahren zur herstellung von dihydromyrcenol | |
| DE2631391B2 (de) | Verfahren zur Herstellung von Alkyladamantanen | |
| DE1068255B (de) | Verfahren zur Herstellung von cyclischen Carbonsäuren und bzw. oder deren Estern aus Cyclododecatrienen-(1,5,9) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |