JPS6121625B2 - - Google Patents
Info
- Publication number
- JPS6121625B2 JPS6121625B2 JP57079256A JP7925682A JPS6121625B2 JP S6121625 B2 JPS6121625 B2 JP S6121625B2 JP 57079256 A JP57079256 A JP 57079256A JP 7925682 A JP7925682 A JP 7925682A JP S6121625 B2 JPS6121625 B2 JP S6121625B2
- Authority
- JP
- Japan
- Prior art keywords
- silica
- formula
- hydrofluoric acid
- aqueous solution
- carried out
- 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 78
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims abstract description 40
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 38
- 239000007864 aqueous solution Substances 0.000 claims abstract description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 14
- 239000003054 catalyst Substances 0.000 claims abstract description 13
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000000243 solution Substances 0.000 claims abstract description 9
- -1 aliphatic nitriles Chemical class 0.000 claims abstract description 8
- 239000004115 Sodium Silicate Substances 0.000 claims abstract description 7
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052911 sodium silicate Inorganic materials 0.000 claims abstract description 7
- 125000003118 aryl group Chemical group 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
- 238000001035 drying Methods 0.000 claims abstract description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 20
- 239000011148 porous material Substances 0.000 claims description 18
- 239000011734 sodium Substances 0.000 claims description 11
- 238000005470 impregnation Methods 0.000 claims description 10
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- IMGQWMPDQYRFAL-UHFFFAOYSA-N n-[[3-(trifluoromethyl)phenyl]methyl]formamide Chemical compound FC(F)(F)C1=CC=CC(CNC=O)=C1 IMGQWMPDQYRFAL-UHFFFAOYSA-N 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- PPECHNDWLRNHEA-UHFFFAOYSA-N n-[3-(trifluoromethyl)phenyl]formamide Chemical compound FC(F)(F)C1=CC=CC(NC=O)=C1 PPECHNDWLRNHEA-UHFFFAOYSA-N 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000001491 aromatic compounds Chemical class 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- DYDNPESBYVVLBO-UHFFFAOYSA-N formanilide Chemical compound O=CNC1=CC=CC=C1 DYDNPESBYVVLBO-UHFFFAOYSA-N 0.000 abstract description 10
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 abstract description 6
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 238000001556 precipitation Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 8
- 150000002825 nitriles Chemical class 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- 239000008187 granular material Substances 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- OGOBINRVCUWLGN-UHFFFAOYSA-N 3-(trifluoromethyl)benzonitrile Chemical compound FC(F)(F)C1=CC=CC(C#N)=C1 OGOBINRVCUWLGN-UHFFFAOYSA-N 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- JOIYKSLWXLFGGR-UHFFFAOYSA-N 2-[3-(trifluoromethyl)phenyl]acetonitrile Chemical compound FC(F)(F)C1=CC=CC(CC#N)=C1 JOIYKSLWXLFGGR-UHFFFAOYSA-N 0.000 description 2
- NWPNXBQSRGKSJB-UHFFFAOYSA-N 2-methylbenzonitrile Chemical compound CC1=CC=CC=C1C#N NWPNXBQSRGKSJB-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- AEKVBBNGWBBYLL-UHFFFAOYSA-N 4-fluorobenzonitrile Chemical compound FC1=CC=C(C#N)C=C1 AEKVBBNGWBBYLL-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- IIBOGKHTXBPGEI-UHFFFAOYSA-N N-benzylformamide Chemical compound O=CNCC1=CC=CC=C1 IIBOGKHTXBPGEI-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- SUSQOBVLVYHIEX-UHFFFAOYSA-N phenylacetonitrile Chemical compound N#CCC1=CC=CC=C1 SUSQOBVLVYHIEX-UHFFFAOYSA-N 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- LJFDXXUKKMEQKE-UHFFFAOYSA-N 2,4-difluorobenzonitrile Chemical compound FC1=CC=C(C#N)C(F)=C1 LJFDXXUKKMEQKE-UHFFFAOYSA-N 0.000 description 1
- YOYAIZYFCNQIRF-UHFFFAOYSA-N 2,6-dichlorobenzonitrile Chemical compound ClC1=CC=CC(Cl)=C1C#N YOYAIZYFCNQIRF-UHFFFAOYSA-N 0.000 description 1
- BNBRIFIJRKJGEI-UHFFFAOYSA-N 2,6-difluorobenzonitrile Chemical compound FC1=CC=CC(F)=C1C#N BNBRIFIJRKJGEI-UHFFFAOYSA-N 0.000 description 1
- AGAOESUOSOGZOD-UHFFFAOYSA-N 2-(2,4-difluorophenyl)acetonitrile Chemical compound FC1=CC=C(CC#N)C(F)=C1 AGAOESUOSOGZOD-UHFFFAOYSA-N 0.000 description 1
- UIMMFRUOZOWROM-UHFFFAOYSA-N 2-(2,5-difluorophenyl)acetonitrile Chemical compound FC1=CC=C(F)C(CC#N)=C1 UIMMFRUOZOWROM-UHFFFAOYSA-N 0.000 description 1
- MRDUURPIPLIGQX-UHFFFAOYSA-N 2-(2-chlorophenyl)acetonitrile Chemical compound ClC1=CC=CC=C1CC#N MRDUURPIPLIGQX-UHFFFAOYSA-N 0.000 description 1
- OYOGNBWWSNXFQI-UHFFFAOYSA-N 2-(2-fluoro-5-methylphenyl)acetonitrile Chemical compound CC1=CC=C(F)C(CC#N)=C1 OYOGNBWWSNXFQI-UHFFFAOYSA-N 0.000 description 1
- DAVJMKMVLKOQQC-UHFFFAOYSA-N 2-(2-fluorophenyl)acetonitrile Chemical compound FC1=CC=CC=C1CC#N DAVJMKMVLKOQQC-UHFFFAOYSA-N 0.000 description 1
- JHQBLYITVCBGTO-UHFFFAOYSA-N 2-(4-fluorophenyl)acetonitrile Chemical compound FC1=CC=C(CC#N)C=C1 JHQBLYITVCBGTO-UHFFFAOYSA-N 0.000 description 1
- COYCHCYSJJZVQR-UHFFFAOYSA-N 2-(5-fluoro-2-methylphenyl)acetonitrile Chemical compound CC1=CC=C(F)C=C1CC#N COYCHCYSJJZVQR-UHFFFAOYSA-N 0.000 description 1
- IVQSJULZJSTFJM-UHFFFAOYSA-N 2-[2-(trifluoromethylsulfanyl)phenyl]acetonitrile Chemical compound FC(F)(F)SC1=CC=CC=C1CC#N IVQSJULZJSTFJM-UHFFFAOYSA-N 0.000 description 1
- ARLVXKPAQOUNTM-UHFFFAOYSA-N 2-[2-chloro-5-(trifluoromethoxy)phenyl]acetonitrile Chemical compound FC(F)(F)OC1=CC=C(Cl)C(CC#N)=C1 ARLVXKPAQOUNTM-UHFFFAOYSA-N 0.000 description 1
- LYFCAROXYJTUQF-UHFFFAOYSA-N 2-[4-(trifluoromethoxy)phenyl]acetonitrile Chemical compound FC(F)(F)OC1=CC=C(CC#N)C=C1 LYFCAROXYJTUQF-UHFFFAOYSA-N 0.000 description 1
- QNKOCFJZJWOXDE-UHFFFAOYSA-N 2-[4-(trifluoromethyl)phenyl]acetonitrile Chemical compound FC(F)(F)C1=CC=C(CC#N)C=C1 QNKOCFJZJWOXDE-UHFFFAOYSA-N 0.000 description 1
- HZIDFDPCOAUCGK-UHFFFAOYSA-N 2-[4-(trifluoromethylsulfanyl)phenyl]acetonitrile Chemical compound FC(F)(F)SC1=CC=C(CC#N)C=C1 HZIDFDPCOAUCGK-UHFFFAOYSA-N 0.000 description 1
- LDKYCZDAPXYENY-UHFFFAOYSA-N 2-[5-chloro-2-(trifluoromethoxy)phenyl]acetonitrile Chemical compound FC(F)(F)OC1=CC=C(Cl)C=C1CC#N LDKYCZDAPXYENY-UHFFFAOYSA-N 0.000 description 1
- LCISFYAQKHOWBP-UHFFFAOYSA-N 2-chloro-5-(trifluoromethyl)benzonitrile Chemical compound FC(F)(F)C1=CC=C(Cl)C(C#N)=C1 LCISFYAQKHOWBP-UHFFFAOYSA-N 0.000 description 1
- NHWQMJMIYICNBP-UHFFFAOYSA-N 2-chlorobenzonitrile Chemical compound ClC1=CC=CC=C1C#N NHWQMJMIYICNBP-UHFFFAOYSA-N 0.000 description 1
- GDHXJNRAJRCGMX-UHFFFAOYSA-N 2-fluorobenzonitrile Chemical compound FC1=CC=CC=C1C#N GDHXJNRAJRCGMX-UHFFFAOYSA-N 0.000 description 1
- NVAOLENBKNECGF-UHFFFAOYSA-N 2-phenylpropanenitrile Chemical compound N#CC(C)C1=CC=CC=C1 NVAOLENBKNECGF-UHFFFAOYSA-N 0.000 description 1
- VIUDTWATMPPKEL-UHFFFAOYSA-N 3-(trifluoromethyl)aniline Chemical compound NC1=CC=CC(C(F)(F)F)=C1 VIUDTWATMPPKEL-UHFFFAOYSA-N 0.000 description 1
- CIIUZJBOSHGHSN-UHFFFAOYSA-N 3-(trifluoromethylsulfanyl)benzonitrile Chemical compound FC(F)(F)SC1=CC=CC(C#N)=C1 CIIUZJBOSHGHSN-UHFFFAOYSA-N 0.000 description 1
- WBUOVKBZJOIOAE-UHFFFAOYSA-N 3-chlorobenzonitrile Chemical compound ClC1=CC=CC(C#N)=C1 WBUOVKBZJOIOAE-UHFFFAOYSA-N 0.000 description 1
- JZTPKAROPNTQQV-UHFFFAOYSA-N 3-fluorobenzonitrile Chemical compound FC1=CC=CC(C#N)=C1 JZTPKAROPNTQQV-UHFFFAOYSA-N 0.000 description 1
- IBUQEIIFTPFARK-UHFFFAOYSA-N 3-phenoxybenzonitrile Chemical compound N#CC1=CC=CC(OC=2C=CC=CC=2)=C1 IBUQEIIFTPFARK-UHFFFAOYSA-N 0.000 description 1
- XWHIXOMWXCHJPP-UHFFFAOYSA-N 4-(trifluoromethoxy)benzonitrile Chemical compound FC(F)(F)OC1=CC=C(C#N)C=C1 XWHIXOMWXCHJPP-UHFFFAOYSA-N 0.000 description 1
- DRNJIKRLQJRKMM-UHFFFAOYSA-N 4-(trifluoromethyl)benzonitrile Chemical compound FC(F)(F)C1=CC=C(C#N)C=C1 DRNJIKRLQJRKMM-UHFFFAOYSA-N 0.000 description 1
- VBPYHJRQZZCFCW-UHFFFAOYSA-N 4-chloro-3-(trifluoromethyl)benzonitrile Chemical compound FC(F)(F)C1=CC(C#N)=CC=C1Cl VBPYHJRQZZCFCW-UHFFFAOYSA-N 0.000 description 1
- GJNGXPDXRVXSEH-UHFFFAOYSA-N 4-chlorobenzonitrile Chemical compound ClC1=CC=C(C#N)C=C1 GJNGXPDXRVXSEH-UHFFFAOYSA-N 0.000 description 1
- IVYMIRMKXZAHRV-UHFFFAOYSA-N 4-chlorophenylacetonitrile Chemical compound ClC1=CC=C(CC#N)C=C1 IVYMIRMKXZAHRV-UHFFFAOYSA-N 0.000 description 1
- CVNOWLNNPYYEOH-UHFFFAOYSA-N 4-cyanophenol Chemical compound OC1=CC=C(C#N)C=C1 CVNOWLNNPYYEOH-UHFFFAOYSA-N 0.000 description 1
- KRZCOLNOCZKSDF-UHFFFAOYSA-N 4-fluoroaniline Chemical compound NC1=CC=C(F)C=C1 KRZCOLNOCZKSDF-UHFFFAOYSA-N 0.000 description 1
- XDJAAZYHCCRJOK-UHFFFAOYSA-N 4-methoxybenzonitrile Chemical compound COC1=CC=C(C#N)C=C1 XDJAAZYHCCRJOK-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- YKNZTUQUXUXTLE-UHFFFAOYSA-N [3-(trifluoromethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(C(F)(F)F)=C1 YKNZTUQUXUXTLE-UHFFFAOYSA-N 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006115 defluorination reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000000017 hydrogel Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- CMRLEIHOFQKMCW-UHFFFAOYSA-N n-(2,6-dichlorophenyl)formamide Chemical compound ClC1=CC=CC(Cl)=C1NC=O CMRLEIHOFQKMCW-UHFFFAOYSA-N 0.000 description 1
- ZUMJTLJZVNIVSA-UHFFFAOYSA-N n-(3-chlorophenyl)formamide Chemical compound ClC1=CC=CC(NC=O)=C1 ZUMJTLJZVNIVSA-UHFFFAOYSA-N 0.000 description 1
- HTKHNPZBVUDSAX-UHFFFAOYSA-N n-(3-fluorophenyl)formamide Chemical compound FC1=CC=CC(NC=O)=C1 HTKHNPZBVUDSAX-UHFFFAOYSA-N 0.000 description 1
- BUPDLPLGFRDHSJ-UHFFFAOYSA-N n-(4-fluorophenyl)formamide Chemical compound FC1=CC=C(NC=O)C=C1 BUPDLPLGFRDHSJ-UHFFFAOYSA-N 0.000 description 1
- SXEVZVMJNXOXIJ-UHFFFAOYSA-N n-(4-methoxyphenyl)formamide Chemical compound COC1=CC=C(NC=O)C=C1 SXEVZVMJNXOXIJ-UHFFFAOYSA-N 0.000 description 1
- DISFLAKPMJNEBK-UHFFFAOYSA-N n-[(2,4-difluorophenyl)methyl]formamide Chemical compound FC1=CC=C(CNC=O)C(F)=C1 DISFLAKPMJNEBK-UHFFFAOYSA-N 0.000 description 1
- VTKLXRYCMDIKMY-UHFFFAOYSA-N n-[(2,5-difluorophenyl)methyl]formamide Chemical compound FC1=CC=C(F)C(CNC=O)=C1 VTKLXRYCMDIKMY-UHFFFAOYSA-N 0.000 description 1
- RUZYSHZMFLFLPF-UHFFFAOYSA-N n-[(2-chlorophenyl)methyl]formamide Chemical compound ClC1=CC=CC=C1CNC=O RUZYSHZMFLFLPF-UHFFFAOYSA-N 0.000 description 1
- MTAMMOGNOGYGIQ-UHFFFAOYSA-N n-[(2-fluoro-5-methylphenyl)methyl]formamide Chemical compound CC1=CC=C(F)C(CNC=O)=C1 MTAMMOGNOGYGIQ-UHFFFAOYSA-N 0.000 description 1
- HSCJOLWJPZNDGT-UHFFFAOYSA-N n-[(2-fluorophenyl)methyl]formamide Chemical compound FC1=CC=CC=C1CNC=O HSCJOLWJPZNDGT-UHFFFAOYSA-N 0.000 description 1
- YDLAQBRNNOLMIH-UHFFFAOYSA-N n-[(4-chlorophenyl)methyl]formamide Chemical compound ClC1=CC=C(CNC=O)C=C1 YDLAQBRNNOLMIH-UHFFFAOYSA-N 0.000 description 1
- MTXKMAASSRHJEZ-UHFFFAOYSA-N n-[(4-fluorophenyl)methyl]formamide Chemical compound FC1=CC=C(CNC=O)C=C1 MTXKMAASSRHJEZ-UHFFFAOYSA-N 0.000 description 1
- RJPQSBCSNJZEBW-UHFFFAOYSA-N n-[(5-fluoro-2-methylphenyl)methyl]formamide Chemical compound CC1=CC=C(F)C=C1CNC=O RJPQSBCSNJZEBW-UHFFFAOYSA-N 0.000 description 1
- UCSLZLQTEBLGCM-UHFFFAOYSA-N n-[[2-(trifluoromethoxy)phenyl]methyl]formamide Chemical compound FC(F)(F)OC1=CC=CC=C1CNC=O UCSLZLQTEBLGCM-UHFFFAOYSA-N 0.000 description 1
- MBNYCCBUXMWXEH-UHFFFAOYSA-N n-[[2-(trifluoromethylsulfanyl)phenyl]methyl]formamide Chemical compound FC(F)(F)SC1=CC=CC=C1CNC=O MBNYCCBUXMWXEH-UHFFFAOYSA-N 0.000 description 1
- BHIGLTOMFBWBKC-UHFFFAOYSA-N n-[[2-chloro-5-(trifluoromethoxy)phenyl]methyl]formamide Chemical compound FC(F)(F)OC1=CC=C(Cl)C(CNC=O)=C1 BHIGLTOMFBWBKC-UHFFFAOYSA-N 0.000 description 1
- XBXQGPBGYXJMEF-UHFFFAOYSA-N n-[[4-(trifluoromethoxy)phenyl]methyl]formamide Chemical compound FC(F)(F)OC1=CC=C(CNC=O)C=C1 XBXQGPBGYXJMEF-UHFFFAOYSA-N 0.000 description 1
- IVPGDMIJBYBNDX-UHFFFAOYSA-N n-[[4-(trifluoromethyl)phenyl]methyl]formamide Chemical compound FC(F)(F)C1=CC=C(CNC=O)C=C1 IVPGDMIJBYBNDX-UHFFFAOYSA-N 0.000 description 1
- QPOCAXLXAISDQP-UHFFFAOYSA-N n-[[4-(trifluoromethylsulfanyl)phenyl]methyl]formamide Chemical compound FC(F)(F)SC1=CC=C(CNC=O)C=C1 QPOCAXLXAISDQP-UHFFFAOYSA-N 0.000 description 1
- XNZRLIHHLGBIMX-UHFFFAOYSA-N n-[[5-chloro-2-(trifluoromethoxy)phenyl]methyl]formamide Chemical compound FC(F)(F)OC1=CC=C(Cl)C=C1CNC=O XNZRLIHHLGBIMX-UHFFFAOYSA-N 0.000 description 1
- TZAZXQZADJAQFS-UHFFFAOYSA-N n-hydroxy-n-methylformamide Chemical compound CN(O)C=O TZAZXQZADJAQFS-UHFFFAOYSA-N 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/08—Halides
- B01J27/12—Fluorides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/20—Preparation of carboxylic acid nitriles by dehydration of carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8109695A FR2505831A1 (fr) | 1981-05-15 | 1981-05-15 | Procede de preparation de nitriles aromatiques ou aliphatiques |
| FR8109695 | 1982-05-15 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5821658A JPS5821658A (ja) | 1983-02-08 |
| JPS6121625B2 true JPS6121625B2 (en]) | 1986-05-28 |
Family
ID=9258492
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57079256A Granted JPS5821658A (ja) | 1981-05-15 | 1982-05-13 | 芳香族又は脂肪族ニトリルの製造方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4438042A (en]) |
| EP (1) | EP0066483B1 (en]) |
| JP (1) | JPS5821658A (en]) |
| AT (1) | ATE10365T1 (en]) |
| BR (1) | BR8202762A (en]) |
| CA (1) | CA1175859A (en]) |
| DE (1) | DE3261270D1 (en]) |
| FR (1) | FR2505831A1 (en]) |
| HU (1) | HU196952B (en]) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0478024U (en]) * | 1990-11-20 | 1992-07-08 |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2505676A1 (fr) * | 1981-05-15 | 1982-11-19 | Rhone Poulenc Spec Chim | Catalyseurs constitues de silice contenant du fluor leur procede de preparation et leur application a la preparation de nitriles |
| FR2620447B1 (fr) * | 1987-09-15 | 1990-01-26 | Sanofi Sa | Procede de preparation du di-n-propylacetonitrile |
| US5108975A (en) * | 1991-01-28 | 1992-04-28 | Phillips Petroleum Company | Composition and method of making high porosity, high strength compositions |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1250165A (fr) * | 1960-02-26 | 1961-01-06 | Basf Ag | Procédé pour la production de nitriles |
| US4324698A (en) | 1980-10-20 | 1982-04-13 | Texaco Inc. | Fluorided cracking catalyst |
-
1981
- 1981-05-15 FR FR8109695A patent/FR2505831A1/fr not_active Withdrawn
-
1982
- 1982-05-03 EP EP82400803A patent/EP0066483B1/fr not_active Expired
- 1982-05-03 DE DE8282400803T patent/DE3261270D1/de not_active Expired
- 1982-05-03 AT AT82400803T patent/ATE10365T1/de not_active IP Right Cessation
- 1982-05-13 BR BR8202762A patent/BR8202762A/pt unknown
- 1982-05-13 JP JP57079256A patent/JPS5821658A/ja active Granted
- 1982-05-14 HU HU821531A patent/HU196952B/hu not_active IP Right Cessation
- 1982-05-14 CA CA000402998A patent/CA1175859A/fr not_active Expired
- 1982-05-14 US US06/378,226 patent/US4438042A/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0478024U (en]) * | 1990-11-20 | 1992-07-08 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0066483B1 (fr) | 1984-11-21 |
| EP0066483A1 (fr) | 1982-12-08 |
| CA1175859A (fr) | 1984-10-09 |
| JPS5821658A (ja) | 1983-02-08 |
| US4438042A (en) | 1984-03-20 |
| ATE10365T1 (de) | 1984-12-15 |
| FR2505831A1 (fr) | 1982-11-19 |
| HU196952B (en) | 1989-02-28 |
| BR8202762A (pt) | 1983-04-19 |
| DE3261270D1 (en) | 1985-01-03 |
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