IL278051B2 - A method for producing a thioalkyl trifluoromethyl compound and a thioalkyl trifluoromethyl halide compound - Google Patents
A method for producing a thioalkyl trifluoromethyl compound and a thioalkyl trifluoromethyl halide compoundInfo
- Publication number
- IL278051B2 IL278051B2 IL278051A IL27805120A IL278051B2 IL 278051 B2 IL278051 B2 IL 278051B2 IL 278051 A IL278051 A IL 278051A IL 27805120 A IL27805120 A IL 27805120A IL 278051 B2 IL278051 B2 IL 278051B2
- Authority
- IL
- Israel
- Prior art keywords
- formula
- trifluoromethylthioalkyl
- atom
- compound
- producing
- Prior art date
Links
- -1 halide compound Chemical class 0.000 title claims description 90
- 238000004519 manufacturing process Methods 0.000 title claims description 82
- 150000001875 compounds Chemical class 0.000 title claims description 55
- 239000000203 mixture Substances 0.000 title claims description 31
- 238000006243 chemical reaction Methods 0.000 claims description 96
- ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 claims description 53
- 239000002904 solvent Substances 0.000 claims description 39
- 125000005843 halogen group Chemical group 0.000 claims description 34
- 238000000034 method Methods 0.000 claims description 31
- 125000000217 alkyl group Chemical group 0.000 claims description 23
- 150000002222 fluorine compounds Chemical class 0.000 claims description 23
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 20
- 229910052801 chlorine Inorganic materials 0.000 claims description 16
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 16
- 238000010438 heat treatment Methods 0.000 claims description 14
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 13
- 229910052740 iodine Inorganic materials 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- 150000004673 fluoride salts Chemical class 0.000 claims description 7
- 150000002825 nitriles Chemical class 0.000 claims description 7
- 229910001515 alkali metal fluoride Inorganic materials 0.000 claims description 6
- 150000001408 amides Chemical class 0.000 claims description 6
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 6
- 150000002170 ethers Chemical class 0.000 claims description 5
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 48
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 39
- 239000002994 raw material Substances 0.000 description 34
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 25
- 239000011698 potassium fluoride Substances 0.000 description 24
- 235000003270 potassium fluoride Nutrition 0.000 description 24
- 239000006227 byproduct Substances 0.000 description 19
- 239000000243 solution Substances 0.000 description 17
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- FNSARZIHZZOLQA-UHFFFAOYSA-N 1-chloro-5-(trifluoromethylsulfanyl)pentane Chemical compound FC(F)(F)SCCCCCCl FNSARZIHZZOLQA-UHFFFAOYSA-N 0.000 description 14
- PHHNNDKXQVKJEP-UHFFFAOYSA-N 1-bromo-5-chloropentane Chemical compound ClCCCCCBr PHHNNDKXQVKJEP-UHFFFAOYSA-N 0.000 description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 125000005037 alkyl phenyl group Chemical group 0.000 description 12
- 238000010992 reflux Methods 0.000 description 12
- YJRRXTCFZOFDSO-UHFFFAOYSA-N 1-bromo-5-(trifluoromethylsulfanyl)pentane Chemical compound BrCCCCCSC(F)(F)F YJRRXTCFZOFDSO-UHFFFAOYSA-N 0.000 description 11
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 11
- IBODDUNKEPPBKW-UHFFFAOYSA-N 1,5-dibromopentane Chemical compound BrCCCCCBr IBODDUNKEPPBKW-UHFFFAOYSA-N 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 230000009257 reactivity Effects 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 9
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 9
- 230000001629 suppression Effects 0.000 description 9
- NBRGGERFCHAAMF-UHFFFAOYSA-N 1,5-bis(trifluoromethylsulfanyl)pentane Chemical compound FC(F)(F)SCCCCCSC(F)(F)F NBRGGERFCHAAMF-UHFFFAOYSA-N 0.000 description 8
- 238000005160 1H NMR spectroscopy Methods 0.000 description 8
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 8
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 8
- 239000003153 chemical reaction reagent Substances 0.000 description 8
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 7
- 239000002585 base Substances 0.000 description 7
- 230000035484 reaction time Effects 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- JTYUIAOHIYZBPB-UHFFFAOYSA-N 1-bromo-6-chlorohexane Chemical compound ClCCCCCCBr JTYUIAOHIYZBPB-UHFFFAOYSA-N 0.000 description 6
- JQJVOCIAMRHGSU-UHFFFAOYSA-N 1-chloro-6-(trifluoromethylsulfanyl)hexane Chemical compound ClCCCCCCSC(F)(F)F JQJVOCIAMRHGSU-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 6
- SKTCDJAMAYNROS-UHFFFAOYSA-N methoxycyclopentane Chemical compound COC1CCCC1 SKTCDJAMAYNROS-UHFFFAOYSA-N 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
- NQVKKRTXPITZQP-UHFFFAOYSA-N 1-bromo-6-(trifluoromethylsulfanyl)hexane Chemical compound BrCCCCCCSC(F)(F)F NQVKKRTXPITZQP-UHFFFAOYSA-N 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 5
- 238000002955 isolation Methods 0.000 description 5
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 description 4
- 241000607479 Yersinia pestis Species 0.000 description 4
- 229940117389 dichlorobenzene Drugs 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 239000011775 sodium fluoride Substances 0.000 description 4
- 235000013024 sodium fluoride Nutrition 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- SGRHVVLXEBNBDV-UHFFFAOYSA-N 1,6-dibromohexane Chemical compound BrCCCCCCBr SGRHVVLXEBNBDV-UHFFFAOYSA-N 0.000 description 3
- GUUHKOCYWBEGGX-UHFFFAOYSA-N 1-chloro-5-iodopentane Chemical compound ClCCCCCI GUUHKOCYWBEGGX-UHFFFAOYSA-N 0.000 description 3
- QTJHNJCILMMRIQ-UHFFFAOYSA-N 1-chloro-6-iodohexane Chemical compound ClCCCCCCI QTJHNJCILMMRIQ-UHFFFAOYSA-N 0.000 description 3
- KNDAEDDIIQYRHY-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-3-(piperazin-1-ylmethyl)pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2)CN1CCNCC1 KNDAEDDIIQYRHY-UHFFFAOYSA-N 0.000 description 3
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KWCCEKVUTKHTMW-UHFFFAOYSA-N Fc1cc(Cl)c(SCC(F)(F)F)cc1OCCCCCSC(F)(F)F Chemical compound Fc1cc(Cl)c(SCC(F)(F)F)cc1OCCCCCSC(F)(F)F KWCCEKVUTKHTMW-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000003905 agrochemical Substances 0.000 description 3
- 235000010290 biphenyl Nutrition 0.000 description 3
- 239000004305 biphenyl Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000009776 industrial production Methods 0.000 description 3
- 238000010813 internal standard method Methods 0.000 description 3
- 150000004694 iodide salts Chemical class 0.000 description 3
- MOVBJUGHBJJKOW-UHFFFAOYSA-N methyl 2-amino-5-methoxybenzoate Chemical compound COC(=O)C1=CC(OC)=CC=C1N MOVBJUGHBJJKOW-UHFFFAOYSA-N 0.000 description 3
- 239000012046 mixed solvent Substances 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 235000017550 sodium carbonate Nutrition 0.000 description 3
- 235000009518 sodium iodide Nutrition 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- VEFLKXRACNJHOV-UHFFFAOYSA-N 1,3-dibromopropane Chemical compound BrCCCBr VEFLKXRACNJHOV-UHFFFAOYSA-N 0.000 description 2
- ULTHEAFYOOPTTB-UHFFFAOYSA-N 1,4-dibromobutane Chemical compound BrCCCCBr ULTHEAFYOOPTTB-UHFFFAOYSA-N 0.000 description 2
- LVWSZGCVEZRFBT-UHFFFAOYSA-N 1,7-dibromoheptane Chemical compound BrCCCCCCCBr LVWSZGCVEZRFBT-UHFFFAOYSA-N 0.000 description 2
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 2
- JXOSPTBRSOYXGC-UHFFFAOYSA-N 1-Chloro-4-iodobutane Chemical compound ClCCCCI JXOSPTBRSOYXGC-UHFFFAOYSA-N 0.000 description 2
- BAJSMHLJMAUVCR-UHFFFAOYSA-N 1-bromo-10-(trifluoromethylsulfanyl)decane Chemical compound FC(F)(F)SCCCCCCCCCCBr BAJSMHLJMAUVCR-UHFFFAOYSA-N 0.000 description 2
- IBYHHJPAARCAIE-UHFFFAOYSA-N 1-bromo-2-chloroethane Chemical compound ClCCBr IBYHHJPAARCAIE-UHFFFAOYSA-N 0.000 description 2
- TYRIZFQFJXKSBI-UHFFFAOYSA-N 1-bromo-3-(trifluoromethylsulfanyl)propane Chemical compound FC(F)(F)SCCCBr TYRIZFQFJXKSBI-UHFFFAOYSA-N 0.000 description 2
- JPQNPJPNMCTTKE-UHFFFAOYSA-N 1-bromo-4-(trifluoromethylsulfanyl)butane Chemical compound FC(F)(F)SCCCCBr JPQNPJPNMCTTKE-UHFFFAOYSA-N 0.000 description 2
- NIDSRGCVYOEDFW-UHFFFAOYSA-N 1-bromo-4-chlorobutane Chemical compound ClCCCCBr NIDSRGCVYOEDFW-UHFFFAOYSA-N 0.000 description 2
- XQNAXKIJIOAQFV-UHFFFAOYSA-N 1-bromo-7-(trifluoromethylsulfanyl)heptane Chemical compound FC(F)(F)SCCCCCCCBr XQNAXKIJIOAQFV-UHFFFAOYSA-N 0.000 description 2
- ZMAOWMBSLZYILL-UHFFFAOYSA-N 1-bromo-7-chloroheptane Chemical compound ClCCCCCCCBr ZMAOWMBSLZYILL-UHFFFAOYSA-N 0.000 description 2
- XZQGZPYHNGEVAG-UHFFFAOYSA-N 1-bromo-8-(trifluoromethylsulfanyl)octane Chemical compound FC(F)(F)SCCCCCCCCBr XZQGZPYHNGEVAG-UHFFFAOYSA-N 0.000 description 2
- MRESICPRNLSPPL-UHFFFAOYSA-N 1-bromo-8-chlorooctane Chemical compound ClCCCCCCCCBr MRESICPRNLSPPL-UHFFFAOYSA-N 0.000 description 2
- JTOZSXKXZGVGCV-UHFFFAOYSA-N 1-chloro-3-(trifluoromethylsulfanyl)propane Chemical compound FC(F)(F)SCCCCl JTOZSXKXZGVGCV-UHFFFAOYSA-N 0.000 description 2
- SFOYQZYQTQDRIY-UHFFFAOYSA-N 1-chloro-3-iodopropane Chemical compound ClCCCI SFOYQZYQTQDRIY-UHFFFAOYSA-N 0.000 description 2
- VRPNZEIRRJEMAN-UHFFFAOYSA-N 1-chloro-4-(trifluoromethylsulfanyl)butane Chemical compound FC(F)(F)SCCCCCl VRPNZEIRRJEMAN-UHFFFAOYSA-N 0.000 description 2
- YNWGTUAGDVMNLT-UHFFFAOYSA-N 1-chloro-7-(trifluoromethylsulfanyl)heptane Chemical compound FC(F)(F)SCCCCCCCCl YNWGTUAGDVMNLT-UHFFFAOYSA-N 0.000 description 2
- IRBNUNIQMLYRCJ-UHFFFAOYSA-N 1-chloro-7-iodoheptane Chemical compound ClCCCCCCCI IRBNUNIQMLYRCJ-UHFFFAOYSA-N 0.000 description 2
- OMDRAAMAEOJMMT-UHFFFAOYSA-N 1-chloro-8-(trifluoromethylsulfanyl)octane Chemical compound FC(F)(F)SCCCCCCCCCl OMDRAAMAEOJMMT-UHFFFAOYSA-N 0.000 description 2
- GPCJORQWYXQSJB-UHFFFAOYSA-N 1-chloro-8-iodooctane Chemical compound ClCCCCCCCCI GPCJORQWYXQSJB-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- MFESCIUQSIBMSM-UHFFFAOYSA-N I-BCP Chemical compound ClCCCBr MFESCIUQSIBMSM-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 2
- 101100020289 Xenopus laevis koza gene Proteins 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 230000031709 bromination Effects 0.000 description 2
- 238000005893 bromination reaction Methods 0.000 description 2
- JPOXNPPZZKNXOV-UHFFFAOYSA-N bromochloromethane Chemical compound ClCBr JPOXNPPZZKNXOV-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010511 deprotection reaction Methods 0.000 description 2
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229940078552 o-xylene Drugs 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 description 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 1
- GTQHJCOHNAFHRE-UHFFFAOYSA-N 1,10-dibromodecane Chemical compound BrCCCCCCCCCCBr GTQHJCOHNAFHRE-UHFFFAOYSA-N 0.000 description 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- YJUUZFWMKJBVFJ-UHFFFAOYSA-N 1,3-dimethylimidazolidin-4-one Chemical compound CN1CN(C)C(=O)C1 YJUUZFWMKJBVFJ-UHFFFAOYSA-N 0.000 description 1
- IRABFLSTCKOJFB-UHFFFAOYSA-N 1,6-bis(trifluoromethylsulfanyl)hexane Chemical compound C(CCCSC(F)(F)F)CCSC(F)(F)F IRABFLSTCKOJFB-UHFFFAOYSA-N 0.000 description 1
- WGAXVZXBFBHLMC-UHFFFAOYSA-N 1,9-dibromononane Chemical compound BrCCCCCCCCCBr WGAXVZXBFBHLMC-UHFFFAOYSA-N 0.000 description 1
- AMJBCNIDVLQCBR-UHFFFAOYSA-N 1-bromo-10-chlorodecane Chemical compound ClCCCCCCCCCCBr AMJBCNIDVLQCBR-UHFFFAOYSA-N 0.000 description 1
- LEWJNYLBKFMXSX-UHFFFAOYSA-N 1-bromo-10-iododecane Chemical compound BrCCCCCCCCCCI LEWJNYLBKFMXSX-UHFFFAOYSA-N 0.000 description 1
- IDWNHZNFMKSHOE-UHFFFAOYSA-N 1-bromo-2-(trifluoromethylsulfanyl)ethane Chemical compound FC(F)(F)SCCBr IDWNHZNFMKSHOE-UHFFFAOYSA-N 0.000 description 1
- HKQCJJOXYWQRFN-UHFFFAOYSA-N 1-bromo-2-iodoethane Chemical compound BrCCI HKQCJJOXYWQRFN-UHFFFAOYSA-N 0.000 description 1
- ITCHTIHSVATQQI-UHFFFAOYSA-N 1-bromo-3-iodopropane Chemical compound BrCCCI ITCHTIHSVATQQI-UHFFFAOYSA-N 0.000 description 1
- GFKIYVSAPHPZEJ-UHFFFAOYSA-N 1-bromo-4-iodobutane Chemical compound BrCCCCI GFKIYVSAPHPZEJ-UHFFFAOYSA-N 0.000 description 1
- FWDOLPSHUHIDGX-UHFFFAOYSA-N 1-bromo-5-iodopentane Chemical compound BrCCCCCI FWDOLPSHUHIDGX-UHFFFAOYSA-N 0.000 description 1
- YIMPISOHWYXINO-UHFFFAOYSA-N 1-bromo-6-iodohexane Chemical compound BrCCCCCCI YIMPISOHWYXINO-UHFFFAOYSA-N 0.000 description 1
- XLIBMGGGNNROIX-UHFFFAOYSA-N 1-bromo-7-iodoheptane Chemical compound BrCCCCCCCI XLIBMGGGNNROIX-UHFFFAOYSA-N 0.000 description 1
- SGHBPXOHQQYDQZ-UHFFFAOYSA-N 1-bromo-8-iodooctane Chemical compound BrCCCCCCCCI SGHBPXOHQQYDQZ-UHFFFAOYSA-N 0.000 description 1
- ZFGCYYYUILJGJI-UHFFFAOYSA-N 1-bromo-9-(trifluoromethylsulfanyl)nonane Chemical compound FC(F)(F)SCCCCCCCCCBr ZFGCYYYUILJGJI-UHFFFAOYSA-N 0.000 description 1
- GRPYAHAFRYQIEX-UHFFFAOYSA-N 1-bromo-9-chlorononane Chemical compound ClCCCCCCCCCBr GRPYAHAFRYQIEX-UHFFFAOYSA-N 0.000 description 1
- YEMQZARGYZZILB-UHFFFAOYSA-N 1-bromo-9-iodononane Chemical compound BrCCCCCCCCCI YEMQZARGYZZILB-UHFFFAOYSA-N 0.000 description 1
- PZYHLENTJZMOQC-UHFFFAOYSA-N 1-bromohexan-1-ol Chemical compound CCCCCC(O)Br PZYHLENTJZMOQC-UHFFFAOYSA-N 0.000 description 1
- FEMPEHAKBDCGHD-UHFFFAOYSA-N 1-bromohexylboronic acid Chemical compound B(C(CCCCC)Br)(O)O FEMPEHAKBDCGHD-UHFFFAOYSA-N 0.000 description 1
- KITZQTGXRDWCKG-UHFFFAOYSA-N 1-bromopentan-1-ol Chemical compound CCCCC(O)Br KITZQTGXRDWCKG-UHFFFAOYSA-N 0.000 description 1
- JXZSGUJVOHRHOF-UHFFFAOYSA-N 1-chloro-10-(trifluoromethylsulfanyl)decane Chemical compound FC(F)(F)SCCCCCCCCCCCl JXZSGUJVOHRHOF-UHFFFAOYSA-N 0.000 description 1
- YJMLTXCVCADMHF-UHFFFAOYSA-N 1-chloro-10-iododecane Chemical compound ClCCCCCCCCCCI YJMLTXCVCADMHF-UHFFFAOYSA-N 0.000 description 1
- WTQNKOJNJFWSRP-UHFFFAOYSA-N 1-chloro-2-(trifluoromethylsulfanyl)ethane Chemical compound FC(F)(F)SCCCl WTQNKOJNJFWSRP-UHFFFAOYSA-N 0.000 description 1
- JTWWWQGSFTWWDL-UHFFFAOYSA-N 1-chloro-2-iodoethane Chemical compound ClCCI JTWWWQGSFTWWDL-UHFFFAOYSA-N 0.000 description 1
- UMWOUFHFLHDNMY-UHFFFAOYSA-N 1-chloro-9-(trifluoromethylsulfanyl)nonane Chemical compound FC(F)(F)SCCCCCCCCCCl UMWOUFHFLHDNMY-UHFFFAOYSA-N 0.000 description 1
- MCUDHXVIWDEUGP-UHFFFAOYSA-N 1-chloro-9-iodononane Chemical compound ClCCCCCCCCCI MCUDHXVIWDEUGP-UHFFFAOYSA-N 0.000 description 1
- AWFYPPSBLUWMFQ-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(1,4,6,7-tetrahydropyrazolo[4,3-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=C2 AWFYPPSBLUWMFQ-UHFFFAOYSA-N 0.000 description 1
- 125000005999 2-bromoethyl group Chemical group 0.000 description 1
- NOLJPCPMOUBRJN-UHFFFAOYSA-N 2-bromoundecanoic acid Chemical compound CCCCCCCCCC(Br)C(O)=O NOLJPCPMOUBRJN-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 230000005526 G1 to G0 transition Effects 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- MTWVZJXJCQVKIX-UHFFFAOYSA-N Oc1cc(SCC(F)(F)F)c(Cl)cc1F Chemical compound Oc1cc(SCC(F)(F)F)c(Cl)cc1F MTWVZJXJCQVKIX-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910001618 alkaline earth metal fluoride Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- TUDWMIUPYRKEFN-UHFFFAOYSA-N bromoiodomethane Chemical compound BrCI TUDWMIUPYRKEFN-UHFFFAOYSA-N 0.000 description 1
- LUNYIIFMFUTZRD-UHFFFAOYSA-N bromomethylsulfanyl(trifluoro)methane Chemical compound FC(F)(F)SCBr LUNYIIFMFUTZRD-UHFFFAOYSA-N 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- PJGJQVRXEUVAFT-UHFFFAOYSA-N chloroiodomethane Chemical compound ClCI PJGJQVRXEUVAFT-UHFFFAOYSA-N 0.000 description 1
- CQQRPMWQQUKPMR-UHFFFAOYSA-N chloromethylsulfanyl(trifluoro)methane Chemical compound FC(F)(F)SCCl CQQRPMWQQUKPMR-UHFFFAOYSA-N 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- FJBFPHVGVWTDIP-UHFFFAOYSA-N dibromomethane Chemical compound BrCBr FJBFPHVGVWTDIP-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 125000000262 haloalkenyl group Chemical group 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000005347 halocycloalkyl group Chemical group 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/14—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/01—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and halogen atoms, or nitro or nitroso groups bound to the same carbon skeleton
- C07C323/02—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and halogen atoms, or nitro or nitroso groups bound to the same carbon skeleton having sulfur atoms of thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/03—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and halogen atoms, or nitro or nitroso groups bound to the same carbon skeleton having sulfur atoms of thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2018084522 | 2018-04-25 | ||
| PCT/JP2019/016449 WO2019208355A1 (ja) | 2018-04-25 | 2019-04-17 | トリフルオロメチルチオアルキル化合物の製造方法及びトリフルオロメチルチオアルキルハライド化合物の組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| IL278051A IL278051A (en) | 2020-11-30 |
| IL278051B1 IL278051B1 (en) | 2023-08-01 |
| IL278051B2 true IL278051B2 (en) | 2023-12-01 |
Family
ID=68294078
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL278051A IL278051B2 (en) | 2018-04-25 | 2019-04-17 | A method for producing a thioalkyl trifluoromethyl compound and a thioalkyl trifluoromethyl halide compound |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JP6660518B1 (zh) |
| CN (1) | CN111699172B (zh) |
| IL (1) | IL278051B2 (zh) |
| TW (1) | TWI719457B (zh) |
| WO (1) | WO2019208355A1 (zh) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2010100307A4 (en) * | 2010-01-04 | 2010-06-03 | Keki Hormusji Gharda | A method for the preparation of perfluoroalkyl sulfenyl chloride |
| CN102516000B (zh) * | 2011-10-27 | 2014-07-23 | 中国科学院上海有机化学研究所 | 一种合成芳基三氟甲巯基化合物的方法 |
| JP6236545B2 (ja) * | 2014-11-12 | 2017-11-22 | クミアイ化学工業株式会社 | トリフルオロメチルチオアルキル化合物の製造方法 |
-
2019
- 2019-04-17 JP JP2019565358A patent/JP6660518B1/ja active Active
- 2019-04-17 WO PCT/JP2019/016449 patent/WO2019208355A1/ja active Application Filing
- 2019-04-17 CN CN201980012615.7A patent/CN111699172B/zh active Active
- 2019-04-17 IL IL278051A patent/IL278051B2/en unknown
- 2019-04-24 TW TW108114227A patent/TWI719457B/zh active
Also Published As
| Publication number | Publication date |
|---|---|
| JP6660518B1 (ja) | 2020-03-11 |
| IL278051B1 (en) | 2023-08-01 |
| WO2019208355A1 (ja) | 2019-10-31 |
| CN111699172B (zh) | 2023-03-24 |
| TWI719457B (zh) | 2021-02-21 |
| CN111699172A (zh) | 2020-09-22 |
| TW201945335A (zh) | 2019-12-01 |
| IL278051A (en) | 2020-11-30 |
| JPWO2019208355A1 (ja) | 2020-04-30 |
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