USRE34423E - Substituted benzenes useful as intermediates - Google Patents
Substituted benzenes useful as intermediates Download PDFInfo
- Publication number
- USRE34423E USRE34423E US07/885,989 US88598992A USRE34423E US RE34423 E USRE34423 E US RE34423E US 88598992 A US88598992 A US 88598992A US RE34423 E USRE34423 E US RE34423E
- Authority
- US
- United States
- Prior art keywords
- sub
- sme
- ome
- reaction
- methyl
- 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 - Lifetime
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- 150000001555 benzenes Chemical class 0.000 title abstract description 23
- 239000000543 intermediate Substances 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 125
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 34
- 238000000034 method Methods 0.000 abstract description 16
- XPNHHPXSCYDOKL-UHFFFAOYSA-N 4-benzoyl-1,2-dihydropyrazol-3-one Chemical compound N1N=CC(C(=O)C=2C=CC=CC=2)=C1O XPNHHPXSCYDOKL-UHFFFAOYSA-N 0.000 abstract description 13
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract description 11
- 229910002091 carbon monoxide Inorganic materials 0.000 abstract description 11
- XBYRMPXUBGMOJC-UHFFFAOYSA-N 1,2-dihydropyrazol-3-one Chemical compound OC=1C=CNN=1 XBYRMPXUBGMOJC-UHFFFAOYSA-N 0.000 abstract description 9
- 239000003054 catalyst Substances 0.000 abstract description 8
- 230000000737 periodic effect Effects 0.000 abstract description 5
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 65
- 239000000460 chlorine Substances 0.000 description 46
- 239000000243 solution Substances 0.000 description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 37
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 36
- 239000002904 solvent Substances 0.000 description 32
- 125000004432 carbon atom Chemical group C* 0.000 description 29
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 28
- 239000000203 mixture Substances 0.000 description 27
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 239000007864 aqueous solution Substances 0.000 description 24
- 229910052740 iodine Inorganic materials 0.000 description 23
- 239000000047 product Substances 0.000 description 23
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 22
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 22
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 20
- 239000012954 diazonium Substances 0.000 description 20
- 229910002092 carbon dioxide Inorganic materials 0.000 description 19
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 18
- 229910052801 chlorine Chemical group 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- 150000003839 salts Chemical group 0.000 description 15
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 14
- 229910052731 fluorine Inorganic materials 0.000 description 14
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 14
- 239000000126 substance Substances 0.000 description 13
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- 150000001448 anilines Chemical class 0.000 description 12
- 125000001309 chloro group Chemical group Cl* 0.000 description 12
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 12
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 12
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical class ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 125000001153 fluoro group Chemical group F* 0.000 description 10
- 239000012044 organic layer Substances 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 125000004093 cyano group Chemical group *C#N 0.000 description 9
- 125000005843 halogen group Chemical group 0.000 description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 9
- 235000010288 sodium nitrite Nutrition 0.000 description 9
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- 229910052794 bromium Inorganic materials 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 7
- 229910002666 PdCl2 Inorganic materials 0.000 description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical class BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 125000001424 substituent group Chemical group 0.000 description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 7
- ZHFTYUGQZOAXFR-UHFFFAOYSA-N 1-bromo-2-chloro-3-(methoxymethyl)-4-methylsulfonylbenzene Chemical compound COCC1=C(Cl)C(Br)=CC=C1S(C)(=O)=O ZHFTYUGQZOAXFR-UHFFFAOYSA-N 0.000 description 6
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 6
- 150000001989 diazonium salts Chemical class 0.000 description 6
- 238000001914 filtration Methods 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- -1 methyl mercapto group Chemical group 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 5
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical class [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 239000005457 ice water Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- KHLKTMJARYUXKF-UHFFFAOYSA-N 1-bromo-2-chloro-3-methyl-4-methylsulfonylbenzene Chemical compound CC1=C(Cl)C(Br)=CC=C1S(C)(=O)=O KHLKTMJARYUXKF-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 101150003085 Pdcl gene Proteins 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- QJANIQCEDPJNLO-UHFFFAOYSA-N (2-methyl-3-nitrophenyl)methanol Chemical compound CC1=C(CO)C=CC=C1[N+]([O-])=O QJANIQCEDPJNLO-UHFFFAOYSA-N 0.000 description 3
- KIIFEJMXDNIUCL-UHFFFAOYSA-N 1-(methoxymethyl)-2-methyl-3-nitrobenzene Chemical compound COCC1=CC=CC([N+]([O-])=O)=C1C KIIFEJMXDNIUCL-UHFFFAOYSA-N 0.000 description 3
- GXQKMZQAWXBWBB-UHFFFAOYSA-N 1-bromo-3-(bromomethyl)-2-chloro-4-methylsulfonylbenzene Chemical compound CS(=O)(=O)C1=CC=C(Br)C(Cl)=C1CBr GXQKMZQAWXBWBB-UHFFFAOYSA-N 0.000 description 3
- UBPOEWHLSICXAF-UHFFFAOYSA-N 3-(methoxymethyl)-2-methylaniline Chemical compound COCC1=CC=CC(N)=C1C UBPOEWHLSICXAF-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 3
- 125000005083 alkoxyalkoxy group Chemical group 0.000 description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 3
- 125000004414 alkyl thio group Chemical group 0.000 description 3
- CIZVQWNPBGYCGK-UHFFFAOYSA-N benzenediazonium Chemical class N#[N+]C1=CC=CC=C1 CIZVQWNPBGYCGK-UHFFFAOYSA-N 0.000 description 3
- 235000010233 benzoic acid Nutrition 0.000 description 3
- 150000001559 benzoic acids Chemical class 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 238000006193 diazotization reaction Methods 0.000 description 3
- 239000003480 eluent Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- VHDXNZRKWAYASH-UHFFFAOYSA-N o-methyl 3-amino-2,6-dimethylbenzenecarbothioate Chemical compound COC(=S)C1=C(C)C=CC(N)=C1C VHDXNZRKWAYASH-UHFFFAOYSA-N 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- 238000010898 silica gel chromatography Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 3
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 3
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 3
- DMEDNTFWIHCBRK-UHFFFAOYSA-N 1,3-dichloro-2-methylbenzene Chemical compound CC1=C(Cl)C=CC=C1Cl DMEDNTFWIHCBRK-UHFFFAOYSA-N 0.000 description 2
- RYMMNSVHOKXTNN-UHFFFAOYSA-N 1,3-dichloro-5-methyl-benzene Natural products CC1=CC(Cl)=CC(Cl)=C1 RYMMNSVHOKXTNN-UHFFFAOYSA-N 0.000 description 2
- DGAYFCFQKDUHQN-UHFFFAOYSA-N 1-bromo-2,4-dichloro-3-methylbenzene Chemical compound CC1=C(Cl)C=CC(Br)=C1Cl DGAYFCFQKDUHQN-UHFFFAOYSA-N 0.000 description 2
- VEKIRHPKUFHYGT-UHFFFAOYSA-N 1-bromo-2-chloro-3-methyl-4-methylsulfanylbenzene Chemical compound CSC1=CC=C(Br)C(Cl)=C1C VEKIRHPKUFHYGT-UHFFFAOYSA-N 0.000 description 2
- QNMYJMZVOFQIRD-UHFFFAOYSA-N 1-chloro-2-methyl-3-methylsulfanylbenzene Chemical compound CSC1=CC=CC(Cl)=C1C QNMYJMZVOFQIRD-UHFFFAOYSA-N 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 2
- QZVRXWBKQJFSLP-UHFFFAOYSA-N 2-ethyl-1h-pyrazol-3-one Chemical compound CCN1NC=CC1=O QZVRXWBKQJFSLP-UHFFFAOYSA-N 0.000 description 2
- ZVSDSBIRXCOCPD-UHFFFAOYSA-N 3-(methoxymethyl)-2-methyl-4-methylsulfanylaniline Chemical compound COCC1=C(C)C(N)=CC=C1SC ZVSDSBIRXCOCPD-UHFFFAOYSA-N 0.000 description 2
- GNAFGGGFCOUBFZ-UHFFFAOYSA-N 3-bromo-2-chloro-6-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=C(Br)C(Cl)=C1C(O)=O GNAFGGGFCOUBFZ-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- JHINUXWJKCFXLQ-UHFFFAOYSA-N [4-amino-2-(methoxymethyl)-3-methylphenyl] thiocyanate Chemical compound COCC1=C(C)C(N)=CC=C1SC#N JHINUXWJKCFXLQ-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000004768 bromobenzenes Chemical class 0.000 description 2
- ODWXUNBKCRECNW-UHFFFAOYSA-M bromocopper(1+) Chemical compound Br[Cu+] ODWXUNBKCRECNW-UHFFFAOYSA-M 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 150000004696 coordination complex Chemical class 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 125000003963 dichloro group Chemical group Cl* 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- CRZGFIMLHZTLGT-UHFFFAOYSA-N methyl 2-methyl-3-nitrobenzoate Chemical compound COC(=O)C1=CC=CC([N+]([O-])=O)=C1C CRZGFIMLHZTLGT-UHFFFAOYSA-N 0.000 description 2
- ONCOTTQGYSGTKV-UHFFFAOYSA-N methyl 3-amino-2-methyl-6-thiocyanatobenzoate Chemical compound COC(=O)C1=C(C)C(N)=CC=C1SC#N ONCOTTQGYSGTKV-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- QARVLSVVCXYDNA-UHFFFAOYSA-N phenyl bromide Natural products BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 229940048181 sodium sulfide nonahydrate Drugs 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 2
- WMDLZMCDBSJMTM-UHFFFAOYSA-M sodium;sulfanide;nonahydrate Chemical compound O.O.O.O.O.O.O.O.O.[Na+].[SH-] WMDLZMCDBSJMTM-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- HNKJADCVZUBCPG-UHFFFAOYSA-N thioanisole Chemical class CSC1=CC=CC=C1 HNKJADCVZUBCPG-UHFFFAOYSA-N 0.000 description 2
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 description 1
- JJRYTJCOOYOVOZ-UHFFFAOYSA-N 1-diphenylphosphanylbutan-2-yl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(CC)CP(C=1C=CC=CC=1)C1=CC=CC=C1 JJRYTJCOOYOVOZ-UHFFFAOYSA-N 0.000 description 1
- XIYVCLTWLDWKPX-UHFFFAOYSA-N 1-iodo-3-(methoxymethyl)-2-methyl-4-methylsulfanylbenzene Chemical compound COCC1=C(C)C(I)=CC=C1SC XIYVCLTWLDWKPX-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- BYHMLZGICSEKIY-UHFFFAOYSA-M 3-amino-2-methylbenzoate Chemical compound CC1=C(N)C=CC=C1C([O-])=O BYHMLZGICSEKIY-UHFFFAOYSA-M 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- SVEHQUXSUIDHFT-UHFFFAOYSA-N 5-iodo-6-methyl-4,6-bis(methylsulfonyl)cyclohexa-2,4-diene-1-carboxylic acid Chemical compound CS(=O)(=O)C1(C)C(C(O)=O)C=CC(S(C)(=O)=O)=C1I SVEHQUXSUIDHFT-UHFFFAOYSA-N 0.000 description 1
- 101100177155 Arabidopsis thaliana HAC1 gene Proteins 0.000 description 1
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- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 description 1
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- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
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- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- WYRXRHOISWEUST-UHFFFAOYSA-K ruthenium(3+);tribromide Chemical compound [Br-].[Br-].[Br-].[Ru+3] WYRXRHOISWEUST-UHFFFAOYSA-K 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
- 239000002002 slurry Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
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- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- RMBAVIFYHOYIFM-UHFFFAOYSA-M sodium methanethiolate Chemical compound [Na+].[S-]C RMBAVIFYHOYIFM-UHFFFAOYSA-M 0.000 description 1
- WBQTXTBONIWRGK-UHFFFAOYSA-N sodium;propan-2-olate Chemical compound [Na+].CC(C)[O-] WBQTXTBONIWRGK-UHFFFAOYSA-N 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- YWWDBCBWQNCYNR-UHFFFAOYSA-N trimethylphosphine Chemical compound CP(C)C YWWDBCBWQNCYNR-UHFFFAOYSA-N 0.000 description 1
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 description 1
- LFNXCUNDYSYVJY-UHFFFAOYSA-N tris(3-methylphenyl)phosphane Chemical compound CC1=CC=CC(P(C=2C=C(C)C=CC=2)C=2C=C(C)C=CC=2)=C1 LFNXCUNDYSYVJY-UHFFFAOYSA-N 0.000 description 1
- WXAZIUYTQHYBFW-UHFFFAOYSA-N tris(4-methylphenyl)phosphane Chemical compound C1=CC(C)=CC=C1P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 WXAZIUYTQHYBFW-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/16—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C317/22—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
-
- 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
- C07C323/09—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 carbon atoms of six-membered aromatic rings of the carbon skeleton
-
- 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
- C07C323/10—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 singly-bound oxygen atoms bound to the same carbon skeleton
- C07C323/18—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 singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/19—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 singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton with singly-bound oxygen atoms bound to acyclic carbon atoms of the carbon skeleton
-
- 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
- C07C323/10—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 singly-bound oxygen atoms bound to the same carbon skeleton
- C07C323/18—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 singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/20—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 singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton with singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
-
- 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
- C07C323/50—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 carboxyl groups bound to the same carbon skeleton
- C07C323/62—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 carboxyl groups bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
- C07D231/24—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms having sulfone or sulfonic acid radicals in the molecule
Definitions
- the present invention relates to a process for producing 4-benzoyl-5-hydroxypyrazoles useful as herbicides and substituted benzene as their starting materials.
- Certain compounds among 4-benzoyl-5-hydroxypyrazole derivatives are known to have herbicidal activities.
- pyrazolate common name
- pyrazoxyfen common name
- benzofenap common name
- Japanese Patent Application No. 061349/1988 reports on 4-benzoyl-5-hydroxypyrazole derivatives which have selectivity for crop plants including not only rice but also corn, wheat, barley and sorghum as well as cotton, beet, soybean and rapeseed.
- the present inventors have conducted researches with an aim to obtain 4-benzoyl-5-hydroxypyrazoles in an industrially advantageous manner and found a new process.
- the present invention has been accomplished on the basis of this discovery.
- the present invention provides a process for producing a 4-benzoyl-5-hydroxypyrazole of the formula III: ##STR4## wherein A is an alkyl group having from 1 to 3 carbon atoms, an allyl group or a propargyl group, B is a hydrogen atom or a methyl group, R 1 is an alkyl group having from 1 to 4 carbon atoms, an alkoxy group having from 1 to 4 carbon atoms, a trifluoromethyl group, a nitro group, a cyano group or a halogen atom, R 2 is a hydrogen atom, an alkyl group having from 1 to 4 carbon atoms, an alkoxy group having from 1 to 4 carbon atoms, a hydroxy group, an alkoxyalkoxy group having from 3 to 6 carbon atoms, an alkoxyalkyl group having from 2 to 5 carbon atoms, an alkoxycarbonyl group having from 2 to 5 carbon atoms, a carboxyl group, a nitro group,
- R 1 is as defined above, provided that when R 1 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group, and when R 1 is an iodine atom X is a diazonium tetrafluoroboron salt group
- R 2 is as defined above, provided that when R 2 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group
- R 3 is as defined above, provided that when R 3 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group, and when R 3 is an iodine atom, X is a diazonium tetrafluoroboron salt group, and when R 3 is an iodine atom, X is a diazonium tetrafluoroboron salt
- the present invention also provides a substituted benzene of the formula I' as a new compound, which is covered by the substituted benzene represented by the formula I: ##STR7## wherein X is a bromine atom, an iodine atom or a diazonium tetrafluoroboron salt group, R 1 is an alkyl group having from 1 to 4 carbon atoms, an alkoxy group having from 1 to 4 carbon atoms, a trifluoromethyl group, .[.a nitro group, a cyano group or a halogen atom, provided that when X is a bromine atom, R 1 is a chlorine atom, and when X is an iodine atom, R 1 is a chlorine atom or a bromine atom, R 3 is an alkylthio group having 1 or 2 carbon atoms, an alkylsulfinyl group having 1 or 2 carbon atoms, an alkanesulfonyl group having
- R 3 is an alkylthio group having 1 or 2 carbon atoms, an alkanesulfonyl group having 1 or 2 carbon atoms, an alkylsulfinyl group having 1 or 2 carbon atoms, a trifluoromethyl group, a nitro group, a cyano group or a halogen atom, provided that when R 3 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group, and when R 1 is an iodine atom, X is a diazonium tetrafluoroboron salt group, R 3 is an alkylthio group having 1 or 2 carbon atoms, an alkanesulfonyl group having 1 or 2 carbon atoms, an alkylsulfinyl group having 1 or 2 carbon atoms, a trifluoromethyl group, a nitro group, a cyano group or a halogen
- the substituents X, R 1 , R 2 , R 3 and R 4 of the substituted benzene of the formula I to be used in the process for the production of a 4-benzoyl-5-hydroxypyrazole of the formula III of the present invention and of the substituted benzene of the formula I' as the novel compound, include, for example, the following substituents:
- the substituents A and B of the 5-hydroxypyrazole of the formula II include, for example, the following substituents:
- the 5-hydroxypyrazole of the formula II is a tautomer of a 5-pyrazolone of the following formula II': ##STR8## wherein A and B are as defined above, and it may be represented by either structural formula:
- substituted benzene of the formula I' can be prepared, for example, by any one of the following reaction schemes: ##STR9##
- R 1 , R 3 , R 4 and X are as defined above.
- Reaction scheme (1) represents a reaction for preparing a substituted bromobenzene from a substituted benzene and bromine.
- Bromine is used preferably in an amount of from 1.0 to 1.5 mols per mol of the substituted benzene.
- an ion-reaction accelerator such as iron-iodine may be employed.
- the solvent may be any solvent so long as it is inert to the reaction.
- chloroform, carbon tetrachloride or acetic acid may be mentioned.
- the reaction temperature is usually from -20° C. to the refluxing temperature of the solvent, preferably from room temperature to 80° C.
- the reaction is usually completed in 30 minutes to 24 hours.
- reaction of the reaction scheme (1) readily proceeds when the substituent R 3 is an electron donative group such as a methyl mercapto group.
- the reaction scheme (2) represents a reaction for preparing a substituted bromobenzene wherein a substituted aniline is diazotized with sodium nitrite in hydrobromic acid to obtain a substituted benzene diazonium salt, which is then decomposed in hydrobromic acid containing copper bromide.
- Sodium nitrite is used preferably in an amount of from 1.0 to 1.5 mols per mol of the substituted aniline.
- Hydrobromic acid may be at least 3.0 mols per mol of the substituted aniline.
- Copper bromide is required to be from 0.01 to 2.0 mols per mol of the substituted aniline.
- the diazotization reaction is conducted usually at a temperature of from -50° to 50° C., preferably from -20° C. to room temperature and is usually completed in 10 minutes to 5 hour.
- the diazonium-decomposition reaction is accomplished usually in 10 minutes to 3 hours at a temperature of from room temperature to the refluxing temperature of hydrobromic acid.
- Reaction scheme (3) represents a reaction for preparing a substituted iodobenzene, wherein a substituted aniline is diazotized with sodium nitrite in hydrochloric acid to obtain a substituted benzene diazonium salt, which is then decomposed in an aqueous potassium iodide solution.
- Sodium nitrite is used preferably in an amount of from 1.0 to 1.5 mols per mol of the substituted aniline.
- Hydrochloric acid may be at least 2.0 mols per mol of the substituted aniline.
- Potassium iodide is required to be from 1.0 to 1.5. mols per mol of the substituted aniline.
- the diazotization reaction is conducted usually from -50° to 50° C., preferably from -20° C. to room temperature and is completed usually in 10 minutes to 5 hours.
- the diazonium-decomposition reaction is completed usually in 10 minutes to 1 hour at a temperature of from room temperature to 100° C.
- the reaction scheme (4) represents a reaction for preparing a substituted benzene diazonium tetrafluoroborate, wherein a substituted aniline is diazotized with sodium nitrite in tetrafluoroboric acid.
- Sodium nitrite is used preferably in an amount of from 1.0 to 1.5 mols per mol of the substituted aniline, and tetrafluoroboric acid may be at least 2.0 mols per mol of the substituted aniline.
- the reaction is conducted usually from -50° to 50° C., preferably from -20° C. to room temperature and is completed usually in 10 minutes to 1 hour.
- Reaction scheme (5) represents a reaction for preparing a substituted methanesulfonylbenzene by oxidizing a substituted methylmercaptobenzene.
- oxidizing agent m-chloroperbenzoic acid, hydrogen peroxide-acetic acid and sodium hypochlorite may, for example, be mentioned.
- the oxidizing agent is required in an amount of at least 2.0 equivalent to the substituted methylmercaptobenzene.
- the solvent may be any solvent so long as it is inert to the reaction.
- the reaction may be conducted in the absence of a solvent.
- the reaction is completed usually in 30 minutes to 24 hours at a temperature of from -20° to 120° C.
- the substituted benzene of the formula I (including the substituted benzene of the formula I') is used usually from 0.1 to 10 mols, preferably from 0.3 to 5 mols, per mol of the 5-hydroxypyrazole.
- Carbon monoxide may be pure gas. However, it may not necessarily be highly pure and may be a gas mixture diluted with an inert gas such as nitrogen gas or carbon dioxide gas.
- the amount of carbon monoxide may be at least one mol per mol of the substituted benzene of the formula I.
- the pressure of carbon monoxide is usually from atmospheric pressure to 150 kg/cm 2 , preferably atmospheric pressure to 100 kg/cm 2 .
- the catalyst of Group VIII of the Periodic Table to be used in the process of the present invention may be a simple substance of metal such as cobalt, palladium, platinum, rhodium, ruthenium, iridium or osmium. Such a metal may be used alone or may be used as supported on a carrier such as graphite, silica gel, alumina, silica-alumina or molecular sieve.
- metal salts such as acetates, carbonates, nitrates, chlorides and bromides may be employed.
- metal salts such as acetates, carbonates, nitrates, chlorides and bromides
- cobalt acetate, palladium acetate, cobalt carbonate, palladium chloride, cobalt chloride and ruthenium bromide may be mentioned.
- the ligand of such a metal complex there may be mentioned, for example, triphenylphosphine, tri-o-tolylphosphine, tri-m-tolylphosphine, tri-p-tolylphosphine, 1,2-bis(diphenylphosphino)butane, tri-n-butylphosphine, triethylphosphine, benzonitrile or carbon monoxide.
- the metal complexes include, for example,
- Co 2 (CO) 8 PdCl 2 (PPh 3 ) 2 , PdBr 2 (PPh 3 ) 2 , Pd(PPh 3 ) 4 ,
- PdCl 2 [P(Ph) 2 CH 2 CH 2 P(Ph) 2 ], PdCl 2 (PhCN) 2 ,
- the ligand may be added to the reaction system in an amount in excess of the amount required for forming a metal complex.
- the catalyst of Group VIII of the Periodic Table is used usually in an amount of from 0.0001 to 150 g atom, preferably from 0.001 to 100 g atom as metal per mol of the substituted benzene of the formula I.
- the base to be used together with the catalyst may be an amine such as triethylamine, tri-n-butylamine, pyridine, dimethylaniline or tetramethylurea, an organic carboxylate such as sodium acetate or potassium propionate, or an inorganic base such as sodium carbonate, potassium carbonate, sodium hydrogencarbonate, calcium oxide, sodium hydroxide, potassium hydroxide or calcium hydroxide.
- the base is used usually in an amount of from 0.1 to 100 mols, preferably from 1.0 to 30 mols per mol of the substituted benzene of the formula I.
- the reaction may be conducted in an inert solvent or in the absence of a solvent.
- the solvent may be an ether such as diethyl ether, diethylene glycol dimethyl ether, tetrahydrofuran or dioxane, an aromatic hydrocarbon such as benzene, toluene, xylene, nitrobenzene or chlorobenzene, a nitrile such as acetonitrile or benzonitrile, N,N-dimethylacetamide, N,N-dimethylformamide, N-methylpyrrolidone, dimethylsulfoxide or hexamethylphosphoramide.
- an ether such as diethyl ether, diethylene glycol dimethyl ether, tetrahydrofuran or dioxane
- an aromatic hydrocarbon such as benzene, toluene, xylene, nitrobenzene or chlorobenzene
- a nitrile such as acetonitrile or benzonitrile
- the reaction temperature is usually from room temperature to 250° C., preferably from 80° to 200° C.
- the reaction time is usually from 0.5 to 300 hours, preferably from 1 to 70 hours.
- reaction solution was added to 300 ml of ice water and extracted with 300 ml of 1,2-dichloroethane.
- reaction solution was returned to room temperature, and 35.5 g (0.25 mol) of methyl iodide was added thereto and stirred. Further, 1 l of water was added thereto, and the mixture was extracted three times with 500 ml of diethyl ether.
- the ether layer was washed twice with water and dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure.
- Boiling point 107°-110° C./10 mmHg.
- Example 1-1 the same treatment as in Example 1-1 was conducted, followed by distillation under reduced pressure to obtain 47.8 g (yield: 95%) of the desired product.
- Boiling point 104.5°-106° C./0.04 mmHg.
- reaction solution was added to 300 ml ice water. Precipitated crystals were collected by filtration, then washed with water and dried to obtain 25.5 g (yield: 100%) of the desired product.
- reaction solution was returned to room temperature, and 30 ml of methanol was gradually added thereto.
- the mixture was reacted for 3 hours under stirring, and then methanol was distilled off.
- a solution comprising 50.0 g of 4-bromo-3-chloro-2-methyl phenyl methylsulfone and 500 g of carbon tetrachloride, was refluxed under heating, and 37.0 g of bromine was dropwise added while irradiating white light.
- the reaction solution was concentrated, and water was added thereto.
- the mixture was extracted with chloroform.
- the extract was washed sequentially with dilute hydrochloric acid and water and dried over sodium sulfate. Then, the solvent was distilled off under reduced pressure to obtain 7.2 g of the desired product.
- the reaction mixture was left to cool, and water was added thereto.
- the solvent was distilled off under reduced pressure.
- reaction solution was added to 1 l of water and neutralized with a 5% sodium carbonate aqueous solution. Chloroform was added thereto, and the oil component was extracted. The chloroform layer was washed with water and a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 29.6 g of the desired product.
- the reaction solution was stirred at 70° C. for further one hour and then left to cool.
- the oil component was extracted with benzene.
- the benzene layer was washed sequentially with water, a saturated sodium hydrogensulfite aqueous solution, water and a saturated sodium chloride aqueous solution. Then, the solvent was distilled off under reduced pressure, and the residue was purified by column chromatography (eluent: benzene) to obtain 30.0 g of the desired product.
- the reaction mixture was left to cool, and then 100 ml of water was added to the reaction solution.
- the mixture was extracted twice with ethyl acetate.
- the ethyl acetate layer was washed sequentially with a saturated sodium hydrogencarbonate aqueous solution, water and a saturated sodium chloride aqueous solution, and then dried over anhydrous sodium sulfate.
- the solvent was then distilled off under reduced pressure.
- the mixture was stirred at room temperature for 3 hours and then put into 1 l of ice water.
- the mixture was neutralized with sodium carbonate and extracted with chloroform.
- the extract was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate.
- the solvent was distilled off to obtain 34.0 g of the desired product. Oily substance.
- the desired product was prepared in accordance with Example 1-4-(7). Melting point: 66°-67° C.
- the desired product was prepared in the same manner as in Example 1-5. Oily substance.
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Abstract
A process for producing a 4-benzoyl-5-hydroxylpyrazole of the formula III: ##STR1## which comprises reacting carbon monoxide and a 5-hydroxypyrazole of the formula II: ##STR2## with a substituted benzene of the formula I: ##STR3## in the presence of a base and a catalyst of Group VIII of the Periodic Table.
Description
This is a division of application Ser. No. 07/360,468 filed on Jun. 2nd, 1989, now U.S. Pat. No. 4,942,246, granted Jul. 17, 1990.
The present invention relates to a process for producing 4-benzoyl-5-hydroxypyrazoles useful as herbicides and substituted benzene as their starting materials.
Certain compounds among 4-benzoyl-5-hydroxypyrazole derivatives are known to have herbicidal activities.
For example, pyrazolate (common name), pyrazoxyfen (common name) and benzofenap (common name) are practically used as herbicides for paddy fields.
Further, Japanese Patent Application No. 061349/1988 reports on 4-benzoyl-5-hydroxypyrazole derivatives which have selectivity for crop plants including not only rice but also corn, wheat, barley and sorghum as well as cotton, beet, soybean and rapeseed.
These herbicides are 4-benzoyl-5-hydroxypyrazoles themselves or their derivatives.
For the production of 4-benzoyl-5-hydroxypyrazoles, there have been known a process for their production from benzoic acids and 5-hydroxypyrazoles (Japanese Unexamined Patent Publication No. 138627/1976) and a process for their production from substituted benzenes, carbon tetrachloride and 5-hydroxypyrazoles (Japanese Unexamined Patent Publication No. 23668/1983).
However, the process for the production from benzoic acids and 5-hydroxypyrazoles are disadvantageous, since it requires expensive benzoic acids. On the other hand, in the process for the production from substituted benzenes, carbon tetrachloride and 5-hydroxypyrazoles, the substituents of the substituted benzenes must be inert to a Friedel-Craft catalyst. Further, the substituents are restricted to electron donative groups in order for the reaction to proceed smoothly.
Therefore, the above processes are not necessarily satisfactory, and an improved process for the production of 4-benzoyl-5-hydroxypyrazoles has been desired.
The present inventors have conducted researches with an aim to obtain 4-benzoyl-5-hydroxypyrazoles in an industrially advantageous manner and found a new process. The present invention has been accomplished on the basis of this discovery.
The present invention provides a process for producing a 4-benzoyl-5-hydroxypyrazole of the formula III: ##STR4## wherein A is an alkyl group having from 1 to 3 carbon atoms, an allyl group or a propargyl group, B is a hydrogen atom or a methyl group, R1 is an alkyl group having from 1 to 4 carbon atoms, an alkoxy group having from 1 to 4 carbon atoms, a trifluoromethyl group, a nitro group, a cyano group or a halogen atom, R2 is a hydrogen atom, an alkyl group having from 1 to 4 carbon atoms, an alkoxy group having from 1 to 4 carbon atoms, a hydroxy group, an alkoxyalkoxy group having from 3 to 6 carbon atoms, an alkoxyalkyl group having from 2 to 5 carbon atoms, an alkoxycarbonyl group having from 2 to 5 carbon atoms, a carboxyl group, a nitro group, a cyano group or a halogen atom, and R3 is an alkylthio group having from 1 or 2 carbon atoms, an alkylsulfinyl group having 1 or 2 carbon atoms, an alkanesulfonyl group having 1 to 2 carbon atoms, a trifluoromethyl group, a nitro group, a cyano group or a halogen atom, which comprises reacting carbon monoxide and a 5-hydroxypyrazole of the formula II: ##STR5## wherein A and B are as defined above, to a substituted benzene of the formula I: ##STR6## .[.wherein X is a bromine atom, an iodine atom or a diazonium tetrafluoroboron salt group, R1 is as defined above, provided that when X is a bromine atom, R1 is a fluorine atom or a chlorine atom, and when X is an iodine atom, R1 is a fluorine atom, a chlorine atom or a bromine atom, R2 is as defined above, provided that when X is a bromine atom, R2 is a fluorine atom or a chlorine atom, and when X is an iodine atom, R2 is a fluorine atom, a chlorine atom or a bromine atom, and R3 is as defined above, provided that when X is a bromine atom, R3 is a fluorine atom or a chlorine atom, and when X is an iodine atom, R3 is a fluorine atom, a chlorine atom or a bromine atom, in the presence of a base and a catalyst of Group VIII of the Periodic Table..]. .Iadd.wherein X is a bromine atom, an iodine atom or a diazonium tetrafluoroboron salt group, R1 is as defined above, provided that when R1 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group, and when R1 is an iodine atom X is a diazonium tetrafluoroboron salt group, R2 is as defined above, provided that when R2 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group, and R3 is as defined above, provided that when R3 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group, and when R3 is an iodine atom, X is a diazonium tetrafluoroboron group, in the presence of a base and a catalyst of Group VIII of the Periodic Table..Iaddend.
The present invention also provides a substituted benzene of the formula I' as a new compound, which is covered by the substituted benzene represented by the formula I: ##STR7## wherein X is a bromine atom, an iodine atom or a diazonium tetrafluoroboron salt group, R1 is an alkyl group having from 1 to 4 carbon atoms, an alkoxy group having from 1 to 4 carbon atoms, a trifluoromethyl group, .[.a nitro group, a cyano group or a halogen atom, provided that when X is a bromine atom, R1 is a chlorine atom, and when X is an iodine atom, R1 is a chlorine atom or a bromine atom, R3 is an alkylthio group having 1 or 2 carbon atoms, an alkylsulfinyl group having 1 or 2 carbon atoms, an alkanesulfonyl group having 1 or 2 carbon atoms, a trifluoromethyl group, a nitro group, a cyano group or a halogen atom, provided that when X is a bromine atom, R3 is a fluorine atom or a chlorine atom, and when X is an iodine atom, R3 is a fluorine atom, a chlorine atom or a bromine atom, and R4 is an alkyl group having from 1 to 4 carbon atoms, an alkoxy group having from 1 to 4 carbon atoms, a hydroxy group, an alkoxyalkoxy group having from 3 to 6 carbon atoms, an alkoxyalkyl group having from 2 to 5 carbon atoms, an alkoxycarbonyl group having from 2 to 5 carbon atoms, a carboxyl group, a nitro group, a cyano group or a halogen atom, provided that when X is a bromine atom, R4 is a fluorine atom or a chlorine atom, and when X is an iodine atom, R4 is a fluorine atom, a chlorine atom or a bromine atom..]. .Iadd.a nitro group, a cyano group or a halogen atom, provided that when R1 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group, and when R1 is an iodine atom, X is a diazonium tetrafluoroboron salt group, R3 is an alkylthio group having 1 or 2 carbon atoms, an alkanesulfonyl group having 1 or 2 carbon atoms, an alkylsulfinyl group having 1 or 2 carbon atoms, a trifluoromethyl group, a nitro group, a cyano group or a halogen atom, provided that when R3 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group, and when R3 is an iodine atom, X is a diazonium tetrafluoroboron salt group, and R4 is an alkyl group having from 1 to 4 carbon atoms, an alkoxy group having from 1 to 4 carbon atoms, a hydroxy group, an alkoxyalkoxy group having from 3 to 6 carbon atoms, an alkoxyalkyl group having from 2 to 5 carbon atoms, an alkoxycarbonyl group having from 2 to 5 carbon atoms, a carboxyl group, nitro group, a cyano group or a halogen atom, provided that when R4 is a bromine atom, X is an iodine atom or a diazonium tetrafluoroboron salt group, and when R4 is an iodine atom, X is a diazonium tetrafluoroboron salt group. .Iaddend.
Now, the present invention will be described in detail with reference to the preferred embodiments.
The substituents X, R1, R2, R3 and R4 of the substituted benzene of the formula I to be used in the process for the production of a 4-benzoyl-5-hydroxypyrazole of the formula III of the present invention and of the substituted benzene of the formula I' as the novel compound, include, for example, the following substituents:
X: Br, I, N2 + ·BF4 -
R1 : Br (provided X=I or N2 + ·BF4 -)
I (provided X=N2 + ·BF4 -), NO2, CN, F, Cl, Me,
Et, n-Pr, i-Pr, OMe, OEt, OPr-n, OPr-i, CF3
R2 : Br (provided X=I or N2 + ·BF4 -)
I (provided X=N2 + ·BF4 -), NO2, CN, F, Cl, H, Me
Et, n-Pr, i-Pr, OMe, OEt, OPr-n, OPr-i, OBu-n,
OBu-s, OBu-i, OBu-t, OH, OCH2 CH2 OMe, OCH2 CH2 OEt,
OCH2 CH2 OPr-n, OCH2 CH2 OPr-i, CH2 OMe, CH2 OEt,
CH2 OPr-n, CH2 OPr-i, CH2 OBu-n, CH2 OBu-s, CH2 OBu-i,
CH2 OBu-t, CO2 Me, CO2 Et, CO2 Pr-n, CO2 Pr-i,
CO2 Bu-n, CO2 Bu-s, CO2 Bu-i, CO2 Bu-t, CO2 H,
R3 : Br (provided X=I or N2 +·BF4 -)
I(provided X=N2 + ·BF4 -), NO2, CN, F, Cl, SMe,
SEt, SO2 Me, SO2 Et, CF3,
R4 : Br (provided X=I or N2 + ·BF4 -)
I (provided X=N2 + ·BF4 -), NO2, CN, F, Cl, Me,
Et, n-Pr,i-Pr, OMe, OEt, OPr-n, OPr-i, OBu-n,
OBu-s, OBu-i, OBu-t, OH, OCH2 CH2 OMe, OCH2 CH2 O Et,
OCH2 CH2 OPr-n, OCH2 CH2 OPr-i, CH2 OMe, CH2 OEt,
CH2 OPr-n, CH2 OPr-i, CH2 OBu-n, CH2 OBu-s, CH2 OBu-i,
CH2 OBu-t, CO2 Me, CO2 Et, CO2 Pr-n, CO2 Pr-i, CO2 Bu-n,
CO2 Bu-s,
CO2 Bu-i, CO2 Bu-t, CO2 H
The substituents A and B of the 5-hydroxypyrazole of the formula II include, for example, the following substituents:
A: Me, Et, N-Pr, i-Pr, CH2 CH=CH2, CH2 C.tbd.CH
B: H, Me
The 5-hydroxypyrazole of the formula II is a tautomer of a 5-pyrazolone of the following formula II': ##STR8## wherein A and B are as defined above, and it may be represented by either structural formula:
Now, the process for producing a substituted benzene of the formula I' as the compound of the present invention, will be described in detail.
Namely, the substituted benzene of the formula I' can be prepared, for example, by any one of the following reaction schemes: ##STR9##
In the above formulas, R1, R3, R4 and X are as defined above.
Reaction scheme (1) represents a reaction for preparing a substituted bromobenzene from a substituted benzene and bromine.
Bromine is used preferably in an amount of from 1.0 to 1.5 mols per mol of the substituted benzene. As a catalyst, an ion-reaction accelerator such as iron-iodine may be employed.
The solvent may be any solvent so long as it is inert to the reaction. For example, chloroform, carbon tetrachloride or acetic acid may be mentioned.
The reaction temperature is usually from -20° C. to the refluxing temperature of the solvent, preferably from room temperature to 80° C.
The reaction is usually completed in 30 minutes to 24 hours.
Generally, the reaction of the reaction scheme (1) readily proceeds when the substituent R3 is an electron donative group such as a methyl mercapto group.
The reaction scheme (2) represents a reaction for preparing a substituted bromobenzene wherein a substituted aniline is diazotized with sodium nitrite in hydrobromic acid to obtain a substituted benzene diazonium salt, which is then decomposed in hydrobromic acid containing copper bromide.
Sodium nitrite is used preferably in an amount of from 1.0 to 1.5 mols per mol of the substituted aniline. Hydrobromic acid may be at least 3.0 mols per mol of the substituted aniline.
Copper bromide is required to be from 0.01 to 2.0 mols per mol of the substituted aniline.
The diazotization reaction is conducted usually at a temperature of from -50° to 50° C., preferably from -20° C. to room temperature and is usually completed in 10 minutes to 5 hour.
The diazonium-decomposition reaction is accomplished usually in 10 minutes to 3 hours at a temperature of from room temperature to the refluxing temperature of hydrobromic acid.
Reaction scheme (3) represents a reaction for preparing a substituted iodobenzene, wherein a substituted aniline is diazotized with sodium nitrite in hydrochloric acid to obtain a substituted benzene diazonium salt, which is then decomposed in an aqueous potassium iodide solution.
Sodium nitrite is used preferably in an amount of from 1.0 to 1.5 mols per mol of the substituted aniline. Hydrochloric acid may be at least 2.0 mols per mol of the substituted aniline.
Potassium iodide is required to be from 1.0 to 1.5. mols per mol of the substituted aniline.
The diazotization reaction is conducted usually from -50° to 50° C., preferably from -20° C. to room temperature and is completed usually in 10 minutes to 5 hours.
The diazonium-decomposition reaction is completed usually in 10 minutes to 1 hour at a temperature of from room temperature to 100° C.
The reaction scheme (4) represents a reaction for preparing a substituted benzene diazonium tetrafluoroborate, wherein a substituted aniline is diazotized with sodium nitrite in tetrafluoroboric acid.
Sodium nitrite is used preferably in an amount of from 1.0 to 1.5 mols per mol of the substituted aniline, and tetrafluoroboric acid may be at least 2.0 mols per mol of the substituted aniline.
The reaction is conducted usually from -50° to 50° C., preferably from -20° C. to room temperature and is completed usually in 10 minutes to 1 hour.
It is also possible to prepare a substituted benzene diazonium tetrafluoroborate by diazotizing a substituted aniline in at least two equivalents of hydrochloric acid instead of tetrafluoroboric acid, to obtain a substituted benzene diazonium salt solution, and then at least an equivalent of tetrafluoroboric acid is added to the diazonium salt solution.
Reaction scheme (5) represents a reaction for preparing a substituted methanesulfonylbenzene by oxidizing a substituted methylmercaptobenzene. As the oxidizing agent, m-chloroperbenzoic acid, hydrogen peroxide-acetic acid and sodium hypochlorite may, for example, be mentioned.
The oxidizing agent is required in an amount of at least 2.0 equivalent to the substituted methylmercaptobenzene.
The solvent may be any solvent so long as it is inert to the reaction. The reaction may be conducted in the absence of a solvent.
The reaction is completed usually in 30 minutes to 24 hours at a temperature of from -20° to 120° C.
Now, the process for the producing the 4-benzoyl-5-hydroxypyrazole of the formula III will be described in detail.
The substituted benzene of the formula I (including the substituted benzene of the formula I') is used usually from 0.1 to 10 mols, preferably from 0.3 to 5 mols, per mol of the 5-hydroxypyrazole.
Carbon monoxide may be pure gas. However, it may not necessarily be highly pure and may be a gas mixture diluted with an inert gas such as nitrogen gas or carbon dioxide gas.
The amount of carbon monoxide may be at least one mol per mol of the substituted benzene of the formula I.
The pressure of carbon monoxide is usually from atmospheric pressure to 150 kg/cm2, preferably atmospheric pressure to 100 kg/cm2. The catalyst of Group VIII of the Periodic Table to be used in the process of the present invention, may be a simple substance of metal such as cobalt, palladium, platinum, rhodium, ruthenium, iridium or osmium. Such a metal may be used alone or may be used as supported on a carrier such as graphite, silica gel, alumina, silica-alumina or molecular sieve.
Further, their metal salts such as acetates, carbonates, nitrates, chlorides and bromides may be employed. For example, cobalt acetate, palladium acetate, cobalt carbonate, palladium chloride, cobalt chloride and ruthenium bromide may be mentioned.
Further, their metal complexes may be mentioned.
As the ligand of such a metal complex, there may be mentioned, for example, triphenylphosphine, tri-o-tolylphosphine, tri-m-tolylphosphine, tri-p-tolylphosphine, 1,2-bis(diphenylphosphino)butane, tri-n-butylphosphine, triethylphosphine, benzonitrile or carbon monoxide. Specific examples of the metal complexes include, for example,
PdCl2 [P(o-Me-Ph)3 ]2, PdCl2 [P(m-Me-Ph)3 ]2,
PdCl2 [P(p-Me-Ph)3 ]2, PdCl2 (PMe3)2,HCo(CO)4,
Co2 (CO)8, PdCl2 (PPh3)2, PdBr2 (PPh3)2, Pd(PPh3)4,
PdCl2 [P(Ph)2 CH2 CH2 P(Ph)2 ], PdCl2 (PhCN)2,
Pd(CO)(PPh3)3, RhCl(PPh3)3, RhCl(CO)(PPh3)2,
Pt(CO)2 (PPh3)2, H4 Ru(CO)12 and Ru3(CO)12.
In some cases, the ligand may be added to the reaction system in an amount in excess of the amount required for forming a metal complex.
The catalyst of Group VIII of the Periodic Table is used usually in an amount of from 0.0001 to 150 g atom, preferably from 0.001 to 100 g atom as metal per mol of the substituted benzene of the formula I.
The base to be used together with the catalyst may be an amine such as triethylamine, tri-n-butylamine, pyridine, dimethylaniline or tetramethylurea, an organic carboxylate such as sodium acetate or potassium propionate, or an inorganic base such as sodium carbonate, potassium carbonate, sodium hydrogencarbonate, calcium oxide, sodium hydroxide, potassium hydroxide or calcium hydroxide. The base is used usually in an amount of from 0.1 to 100 mols, preferably from 1.0 to 30 mols per mol of the substituted benzene of the formula I.
The reaction may be conducted in an inert solvent or in the absence of a solvent.
The solvent may be an ether such as diethyl ether, diethylene glycol dimethyl ether, tetrahydrofuran or dioxane, an aromatic hydrocarbon such as benzene, toluene, xylene, nitrobenzene or chlorobenzene, a nitrile such as acetonitrile or benzonitrile, N,N-dimethylacetamide, N,N-dimethylformamide, N-methylpyrrolidone, dimethylsulfoxide or hexamethylphosphoramide.
The reaction temperature is usually from room temperature to 250° C., preferably from 80° to 200° C.
The reaction time is usually from 0.5 to 300 hours, preferably from 1 to 70 hours.
Now, the preparation of the substituted benzene of the formula I is described in detail with reference to Examples. However, it should be understood that the present invention is by no means restricted by these specific Examples.
To a solution of 48.8 g (0.3 mol) of 2,6-dichlorotoluene in 60 ml of carbon tetrachloride, 0.7 g of iron powder and 0.1 g of iodine were added. Then, 52.8 g (0.33 mol) of bromine was dropwise added thereto at room temperature while maintaining the reaction temperature at a level of from 22° to 25° C. After completion of the dropwise addition, the reaction was continued at the same temperature until generation of hydrogen bromide ceased.
After the reaction, the reaction solution was added to 300 ml of ice water and extracted with 300 ml of 1,2-dichloroethane.
The organic layer was separated and washed sequentially with water, a saturated sodium hydrogen sulfite aqueous solution, water and a saturated sodium chloride aqueous solution. Then, the solvent was distilled off under reduced pressure to obtain 71.9 g (yield: 99.5%) of desired 2,4-dichloro-3-methylbromobenzene.
Melting point: 32°-33° C.
To a solution of 161 g (1 mol) of 2,6-dichlorotoluene in 700 ml of hexamethylphosphoramide, 105 g (1.5 mol) of sodium methanethiolate was added, and the mixture was reacted at 100° C. for 30 minutes.
After the reaction, the reaction solution was returned to room temperature, and 35.5 g (0.25 mol) of methyl iodide was added thereto and stirred. Further, 1 l of water was added thereto, and the mixture was extracted three times with 500 ml of diethyl ether.
The ether layer was washed twice with water and dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure.
Then, distillation under reduced pressure was conducted to obtain 132.8 g (yield: 77%) of the desired product.
Boiling point: 107°-110° C./10 mmHg.
34.5 g (0.2 mol) of 3-chloro-2 methylphenyl methyl sulfide was dissolved in 50 ml of carbon tetrachloride, and 0.5 g of iron powder and 0.1 g of iodine were added thereto. Then, 35.2 g (0.22 mol) of bromine was dropwise added at a reaction temperature of 30° C. Thereafter, the reaction was continued at the same temperature until generation of hydrogen bromide ceased.
Then, the same treatment as in Example 1-1 was conducted, followed by distillation under reduced pressure to obtain 47.8 g (yield: 95%) of the desired product.
Boiling point: 104.5°-106° C./0.04 mmHg.
To 23.6 g (0.09 mol) of 4-bromo-3-chloro-2-methylphenyl methyl sulfide, 50 ml of a 35% hydrogen peroxide aqueous solution and 50 ml of acetic acid were added, and the mixture was reacted at 80° C. for 4 hours.
After the reaction, the reaction solution was added to 300 ml ice water. Precipitated crystals were collected by filtration, then washed with water and dried to obtain 25.5 g (yield: 100%) of the desired product.
Melting point: 144°-145° C.
10.0 g (35 mmol) of 4-bromo-3-chloro-2-methylphenyl methyl sulfone was added to 150 ml of acetic acid to obtain a uniform solution at 80° C. Thereto, 31.6 g (0.2 mol) of potassium permanganate was portionwise added to maintain the reaction temperature at a level of not higher than 85° C., and the reaction was conducted.
From the reaction solution, acetic acid was distilled off under reduced pressure. Then, 200 ml of a 5% potassium hydroxide aqueous solution was added, and insoluble substances were separated by filtration. To the aqueous solution thus obtained, concentrated hydrochloric acid was added to adjust the pH to a level of not higher than 1, and water was distilled off under reduced pressure. To the residue, ethyl acetate was added, and insoluble salts were separated by filtration. Then, the solvent was distilled off under reduced pressure to obtain 3.7 g of the desired product.
Characteristics: glassy solid
1 H NMR (ε, ppm, CDCl3 -DMSO-d6):
3.22(3H, s), 7.9(2H, A-Bq), 8.73(1H,s)
To 3.7 g of 3-bromo-2-chloro-6-methanesulfonylbenzoic acid, 10 ml of thionyl chloride and 0.1 g of N,N-dimethylformamide were added, and the mixture was reacted for 2 hours at the refluxing temperature. Then, toluene was added thereto, and excess thionylchloride was distilled off.
The reaction solution was returned to room temperature, and 30 ml of methanol was gradually added thereto. The mixture was reacted for 3 hours under stirring, and then methanol was distilled off.
The residue was dissolved in ethyl acetate and washed sequentially with water and a saturated sodium chloride aqueous solution. Then, the solvent was distilled off to obtain 3.72 g of the desired product.
Melting point: 67°-69° C.
A solution comprising 50.0 g of 4-bromo-3-chloro-2-methyl phenyl methylsulfone and 500 g of carbon tetrachloride, was refluxed under heating, and 37.0 g of bromine was dropwise added while irradiating white light.
After completion of the dropwise addition, refluxing was continued under heating for further 3 hours while irradiating white light. The reaction mixture was left to cool, and then chloroform was added thereto. The organic layer was separated and washed sequentially with a aqueous sodium hydrogensulfite solution and water. The organic layer was dried over sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 63.5 g of the desired product.
To a suspension comprising 8.5 g of 4-bromo-2-bromomethyl-3-chlorophenyl methyl sulfone and 100 ml of methanol, 1.5 g of sodium methoxide (95%) was added under cooling with ice, and then the mixture was stirred at room temperature overnight.
The reaction solution was concentrated, and water was added thereto. The mixture was extracted with chloroform. The extract was washed sequentially with dilute hydrochloric acid and water and dried over sodium sulfate. Then, the solvent was distilled off under reduced pressure to obtain 7.2 g of the desired product.
39.0 g (0.2 mol) of methyl 2-methyl-3-nitrobenzoate was dissolved in 600 ml of tert-butanol. Then, 19.0 g of sodium borohydride was added thereto, and 150 ml of methanol was further dropwise added over a period of one hour at the refluxing temperature. Further, refluxing was continued for one hour to complete the reaction.
The reaction mixture was left to cool, and water was added thereto. The solvent was distilled off under reduced pressure.
To the residue, water and chloroform were added. The organic layer was separated and dried over anhydrous sodium sulfate. Further, the solvent was distilled off to obtain 30.7 g of 2-methyl-3-nitrobenzyl alcohol.
To the reaction solution, water was added. The organic layer were separated and washed sequentially with water, a 2% hydrochloric acid aqueous solution, water and a saturated sodium chloride aqueous solution. Then, the solvent was distilled off to obtain 30.9 g of 2-methyl-3-nitrobenzyl methyl ether. Oily substance.
To 30.7 g (0.17 mol) of the above 2-methyl-3-nitrobenzyl methyl ether, 200 ml of methanol was added and dissolved. Then, 92 ml of concentrated hydrochloric acid was gradually added. Then, 30.4 g of iron powder was gradually added so that the reaction temperature became not higher than 60° C., and the reaction was continued for further one hour.
To the reaction solution, 300 ml of water was added, and sodium hydroxide was added until the solution became at least pH 8.
To the slurry thereby obtained, chloroform was added and thoroughly stirred. Then, solid was separated by filtration. From the filtrate, the organic layer was separated. This organic layer was washed sequentially with water and a saturated sodium chloride aqueous solution, and then dried over anhydrous sodium sulfate. Further, the solvent was distilled off under reduced pressure to obtain 23.1 g of 3-methoxymethyl-2-methylaniline. Oily substance.
22.6 g (0.15 mol) of 3-methoxymethyl-2-methylaniline was dissolved in 300 ml of methanol, and then 36.5 g of sodium thiocyanate was added to obtain a uniform solution. This solution was cooled to 0° C., and a solution of 25.2 g of bromine in 100 ml of sodium bromide-saturated methanol, was dropwise added thereto so that the reaction temperature did not exceed 5° C. After the dropwise addition, stirring was continued for one hour at a temperature of not higher than 5° C. and further at room temperature for one hour to complete the reaction.
The reaction solution was added to 1 l of water and neutralized with a 5% sodium carbonate aqueous solution. Chloroform was added thereto, and the oil component was extracted. The chloroform layer was washed with water and a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 29.6 g of the desired product.
29.1 g (0.14 mol) of 3-methoxymethyl-2-methyl-4-thiocyanoaniline was dissolved in 200 ml of ethanol and mixed with an aqueous solution comprising 33.6 g of sodium sulfide nonahydrate and 100 ml of water at room temperature.
Then, 21.9 g of methyl iodide was dropwise added thereto, and the mixture was reacted at room temperature for 3 hours.
After completion of the reaction, the solvent was distilled off under reduced pressure, and the residue was concentrated. Water and chloroform were added thereto, and the organic layer was separated. The organic layer thus obtained was washed sequentially with water and a saturated sodium chloride aqueous solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 25.6 g of the desired product. Oily substance.
To 25.6 g (0.13 mol) of 3-methoxymethyl-2-methyl-4-methylthioaniline, 100 ml of water and 33 ml of concentrated hydrochloric acid were added to obtain an aniline hydrochloride. Then, this solution was cooled to 0° C. and a solution of 9.3 g of sodium nitrite in 30 ml of water, was dropwise added so that the reaction temperature did not exceed 5° C. After completion of the dropwise addition, the stirring was continued for further 30 minutes to complete the diazotization.
A solution of 33 g of potassium iodide in 100 ml of water, was heated to 70° C., and the aqueous solution of the diazonium salt obtained above was gradually added and decomposed. The reaction solution was stirred at 70° C. for further one hour and then left to cool. The oil component was extracted with benzene. The benzene layer was washed sequentially with water, a saturated sodium hydrogensulfite aqueous solution, water and a saturated sodium chloride aqueous solution. Then, the solvent was distilled off under reduced pressure, and the residue was purified by column chromatography (eluent: benzene) to obtain 30.0 g of the desired product.
Melting point: 56.0°-59.0° C.
To 3.08 g of 3'-iodo-2'-methyl-6'-methylthiobenzyl methyl ether, 10 ml of acetic acid and 10 ml of a 35% hydrogen peroxide aqueous solution were added, and the mixture was reacted at 60° C. for 5 hours.
The reaction mixture was left to cool, and then 100 ml of water was added to the reaction solution. The mixture was extracted twice with ethyl acetate. The ethyl acetate layer was washed sequentially with a saturated sodium hydrogencarbonate aqueous solution, water and a saturated sodium chloride aqueous solution, and then dried over anhydrous sodium sulfate. The solvent was then distilled off under reduced pressure. The residue thereby obtained was purified by silica gel column chromatography (eluent: chloroform/ethyl acetate=19/1) to obtain 3.05 g of the desired product.
Melting point: 77°-78° C.
40 g of methyl 2-methyl-3-nitrobenzoate was dissolved in 120 ml of methanol, and 157 g of concentrated hydrochloric acid was added thereto. Then, while maintaining the mixture at the temperature of not higher than 60° C., 36.8 g of iron powder was gradually added in small portions. The mixture was stirred at room temperature for 4 hours and then put into 1 l of ice water. The mixture was neutralized with sodium carbonate and extracted with chloroform (insolubles were removed by filtration in this process). The extract was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 27.8 g of the desired product. Oily substance.
A solution comprising 27.7 g of methyl 3-amino-2-methyl benzoate, 41.5 g of sodium thiocyanate and 250 ml of methanol, was maintained at a temperature of not higher than 0° C., and a solution comprising 100 ml of a sodium bromide-saturated methanol and 28.1 g of bromine was gradually dropwise added thereto. The mixture was stirred at room temperature for 3 hours and then put into 1 l of ice water. The mixture was neutralized with sodium carbonate and extracted with chloroform. The extract was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 34.0 g of the desired product. Oily substance.
To a solution comprising 39.5 g of sodium sulfide nonahydrate and 110 ml of water, a solution comprising 32.9 g of methyl 3-amino-2-methyl-6-thiocyanobenzoate and 300 ml of ethanol, was dropwise added. The mixture was stirred at room temperature for 1.5 hours, and then 24 g of methyl iodide was dropwise added thereto under cooling with ice. The mixture was stirred at room temperature for 2 hours and then concentrated under reduced pressure. A saturated sodium chloride aqueous solution was added thereto, and the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off to obtain 30.1 g of the desired product. Oily substance.
28 g of methyl 3-amino-2-methyl-6-methylthiobenzoate was stirred in 150 ml of concentrated hydrochloric acid at room temperature for 2 hours to obtain its hydrochloride. Then, while maintaining the temperature at a level of not higher than 0° C., a solution comprising 11.9 g of sodium nitrite and 20 ml of water, was dropwise added to obtain a diazonium salt solution. A solution comprising 28.4 g of potassium iodide and 90 ml of water, was maintained at 80° C., and the diazonium salt solution was dropwise added thereto. After completion of the dropwise addition, the mixture was stirred at 80° C. for 15 minutes and then left to cool. Water was added thereto, and the mixture was extracted with chloroform. The extract was washed with an aqueous sodium hydrogensulfite solution and water and then dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 40 g of a crude of the desired product. The crude was purified by silica gel chromatography (developed with benzene) to obtain 36.0 g of the desired product. Oily substance.
The desired product was prepared in accordance with Example 1-4-(7). Melting point: 66°-67° C.
16.1 g of methyl 3-amino-2-methyl-6-methylthiobenzoate was stirred in 150 ml of hydrobromic acid (48%) to obtain its hydrobromide. While maintaining the temperature at a level of not higher than 0° C., a solution comprising 7.2 g of sodium nitrite and 20 ml of water, was dropwise added to obtain a diazonium salt solution.
A solution comprising 6.0 g of cuprous bromide and 7.7 g of hydrobromic acid (48%) was refluxed under heating, and the diazonium salt solution was dropwise added thereto. After completion of the dropwise addition, the mixture was refluxed under heating for further one hour and then left to cool. Ice water was added thereto, and the mixture was extracted with chloroform. The extract was washed with an aqueous sodium-hydrogen sulfite solution and water, and then dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 19.2 g of a crude of the desired product. The crude was purified by silica gel column chromatography (eluent: benzene) to obtain 17.1 g of the purified desired product. Oily substance.
The desired product was prepared in the same manner as in Example 1-5. Oily substance.
To a suspension comprising 20.0 g of 4-bromo-2-bromomethyl-3-chlorophenyl methyl sulfone and 200 ml of isopropanol, 100 ml of an isopropanol solution of sodium isopropoxide (prepared from 1.4 g of metal sodium) was added at room temperature, and the mixture was stirred overnight. The post treatment was conducted in the same manner as in Example 1-3-(2) to obtain 18.4 of the desired product.
Melting point: 87°-91° C.
In Table 1, the physical properties of the substituted benzenes of the formula I will be given.
TABLE 1 ______________________________________ ##STR10## Comp. No. X R.sup.1 R.sup.2 R.sup.3 m.p. (°C.) ______________________________________ 1 I CN H SMe 189˜194 2 I OMe H SMe Oily 3 I NO.sub.2 H CF.sub.3 Oily 4 Br Cl CO.sub.2 Me SO.sub.2 Me 67˜69 5 Br Cl CO.sub.2 H SO.sub.2 Me Oily 6 I Cl CO.sub.2 Me SMe Oily 7 I Cl CO.sub.2 H SMe 155˜159 8 I Cl CO.sub.2 Pr-i SMe Oily 9 Br Me CO.sub.2 Me SMe Oily 10 Br Me CO.sub.2 H SMe 98˜103 11 Br Me CO.sub.2 Pr-i SMe Oily 12 I Me CO.sub.2 Me SMe Oily 13 I Me CO.sub.2 Me SO.sub.2 Me 66˜67 14 I Me CO.sub.2 Et SMe Oily 15 I Me CO.sub.2 Pr-i SMe Oily 16 I Me CO.sub.2 CH.sub. 2 CH.sub.2 OMe SMe Oily 17 I Me CO.sub.2 CH.sub.2 CH.sub.2 Cl SMe Oily 18 I OMe CO.sub.2 Me SMe 78˜80 19 Br Cl CH.sub.2 OMe SO.sub.2 Me 72˜74 20 I Cl CH.sub.2 OMe SMe 53˜56 21 I Me CH.sub.2 OMe SO.sub.2 Me 77˜78 22 I Me CH.sub.2 OMe SMe 56˜59 23 I Me CH.sub.2 OEt SMe Oily 24 I Me CH.sub.2 OPr-i SMe Oily 25 I OMe CH.sub.2 OMe SMe Oily 26 I Me CHMeOMe SMe Oily 27 I Me CHMeOEt SMe Oily 28 I Me CHEtOMe SMe Oily 29 I Me OMe SMe Oily 30 I Cl Cl SMe Oily 31 I Me NO.sub.2 SMe bp. 135˜145° C./ 0.1 mmHg 32 Br Cl Me SO.sub.2 Me 144˜145 33 Br Cl Me SMe bp. 102˜105° C./ 0.03 mmHg 34 I Cl CN Cl 139˜144 35 Br Cl Me Cl Oily 36 Br Cl CH.sub.2 OPr-i SO.sub.2 Me 87˜91 ______________________________________
Now, the process for producing the 4-benzoyl-5-hydroxypyrazole of the formula III derived from the substituted benzene of the formula I, will be described with reference to Examples. However, it should be understood that the present invention is by no means restricted by such specific Examples.
2.0 g of 3-methoxymethyl-2-methyl-4-methylthioiodobenzene, 1.46 g of 1-ethyl-5-hydroxypyrazole, 0.65 g of triethylamine, 4.04 g of anhydrous potassium carbonate, 0.28 g of dichloro(bistriphenylphosphine)palladium and 50 ml of 1,4-dioxane were charged into a 100 ml of Hastelloy autoclave equipped with a rotary stirrer, and the interior of autoclave was substituted with carbon monoxide, then, carbon monoxide was injected under a pressure of 10 kg/cm2. Then, the temperature was gradually raised under stirring, and the reaction was continued at 140° C. for 8 hours. The reaction mixture was left to cool, and then unreacted carbon monoxide was purged. The reaction solution was taken out, and the solvent was distilled off under reduced pressure. Then, water and chloroform were added, and the mixture was subjected to liquid separation. The aqueous layer was washed with chloroform, and insoluble substances were separated by filtration. Concentrated hydrochloric acid was added to bring the pH to a level of not higher than 1. Then, chloroform was added thereto, and the mixture was extracted twice. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure to obtain 1.75 g of a crude of the desired product (yield: 84%). Oily substance.
1.42 g of 2-chloro-4-methanesulfonyl-3-methylbromobenzene, 2.24 g of 1-ethyl-5-hydroxypyrazole, 10 ml of triethylamine, 0.175 g of dichloro(bistriphenylphosphine)palladium and 50 ml of dry 1,4-dioxane were charged into a 100 ml stainless steel autoclave equipped with a rotary stirrer, and the interior of the autoclave was substituted by carbon monoxide. Then, carbon monoxide was injected under a pressure of 20 kg/cm2. Then, the reaction temperature was raised to 150° C. under stirring, and the reaction was continued for 9 hours. The reaction mixture was left to cool and treated in the same manner as in Example 2-1 to obtain 0.60 g of the desired product (yield: 43%).
Melting point: 225°-227° C.
In the following Tables 2 to 5, Examples of the present invention under various conditions will be given.
Further, the physical properties of the 4-benzoyl-5-hydroxypyrazoles of the formula III will be given in Table 6.
TABLE 2 __________________________________________________________________________ ##STR11## ##STR12## Solvent CO pressure Conversion Isolated yield Ex. No. (50 ml) Base (mmol) (kg/cm.sup.2) Temp. (°C.) Time (hr) (%*) (%*) __________________________________________________________________________ 2-3 dioxane Et.sub.3 N(72) 50 150 4.5 100 60 2-4 dioxane Et.sub.3 N(72) 50 120 20 100 55 2-5 dioxane Et.sub.3 N(72) 50 100 18 61 29 2-6 dioxane Et.sub. 3 N(20) 20 150 7 100 62 K.sub.2 CO.sub.3 (10) 2-7 dioxane Et.sub.3 N(20) 50 150 7.5 100 50 K.sub.2 CO.sub.3 (10) 2-8 CH.sub.3 CN Et.sub.3 N(72) 100 100 14 100 85 2-9 HMPA Et.sub.3 N(72) 100 100 3 100 -- 2-10 HMPA Et.sub.3 N(5.5) 100 100 2 100 -- 2-11 1-methyl-2- Et.sub.3 N(72) 100 100 7 70 -- pyrrolidone __________________________________________________________________________ 5 mmol of I1, 20 mmol of II1 and 0.25 mmol of PdCl.sub.2 (PPh.sub.3).sub. were used. *The conversion and the isolated yield were calculated base on I1.
TABLE 3 ______________________________________ ##STR13## ##STR14## ##STR15## Ex. Time Conversion Isolated yield No. B (hr) (%*) (%*) ______________________________________ 2-12 H 18 70 42 2-13 Me 8 35 30 ______________________________________ I-1: 5 mmol, II2: 20 mmol, PdCl.sub.2 (PPh.sub.3).sub.2 : 0.25 mmol, Et.sub.3 N: 72 mmol, CH.sub.3 CN: 50 ml. CO pressure: 100 kg/cm.sup.2, Reaction temp.: 100° C. *based on I1.
TABLE 4 ______________________________________ ##STR16## ##STR17## ##STR18## Ex. Time Conversion Isolated yield No. X (hr) (%*) (%*) ______________________________________ 2-14 Br 24 97 68 2-15 I 5 100 -- ______________________________________ I-1: 5 mmol, II1: 20 mmol, PdCl.sub.2 (PPh.sub.3).sub.2 : 0.25 mmol, Et.sub.3 N: 72 mmol, CH.sub.3 CN: 50 ml. CO pressure: 100 kg/cm.sup.2, Reaction temp.: 100° C. *Base on I2.
TABLE 5 ______________________________________ ##STR19## ##STR20## ##STR21## Ex. Solvent Time Conversion No. X R.sup.2 (50 ml) (hr) (%*) ______________________________________ 2-16 Br Cl dioxane 10 80 2-17 I Me CH.sub.3 CN 5 100 ______________________________________ I-3: 5 mmol, II1: 20 mmol, PdCl.sub.2 (PPh.sub.3).sub.2 : 0.25 mmol, Et.sub.3 N: 72 mmol, CH.sub.3 CN: 50 ml. CO Pressure: 100 kg/cm.sup.2, Reaction temp.: 100° C. *Based on I3.
TABLE 6 ______________________________________ ##STR22## A B R.sup.1 R.sup.2 R.sup.3 m.p. (° C.) ______________________________________ Me H Me CH.sub.2 OMe SO.sub.2 Me Oily Et H Me CH.sub.2 OMe SO.sub.2 Me 116˜118 i-Pr H Me CH.sub.2 OMe SO.sub.2 Me Oily Me H Me CO.sub.2 H SO.sub.2 Me 274˜274.5 Me H Me CO.sub.2 Me SO.sub.2 Me 199˜201 Et H Me CO.sub.2 Me SO.sub.2 Me 150˜152 Me H Me CO.sub.2 Et SO.sub.2 Me 174˜174.5 Et H Me CO.sub.2 Et SO.sub.2 Me 78˜81 Me H Me CO.sub.2 Pr-i SO.sub.2 Me 192˜194 Et H Me CO.sub.2 Pr-i SO.sub.2 Me 125˜128 Me H Cl CO.sub.2 Me Cl 123˜126 Me H Me CH.sub.2 OEt SO.sub.2 Me 178˜179 Et H Me CH.sub.2 OEt SO.sub.2 Me Oily i-Pr H Me CH.sub.2 OEt SO.sub.2 Me Oily Me Me Me CH.sub.2 OEt SO.sub.2 Me Oily Me H Me CHMeOMe SO.sub.2 Me 238˜240 Et H Me CHMeOMe SO.sub.2 Me 138˜141 Me H Cl CH.sub.2 OMe SO.sub.2 Me 189˜190 Et H Cl CH.sub.2 OMe SO.sub.2 Me 151˜154 i-Pr H Cl CH.sub.2 OMe SO.sub.2 Me 142˜144 Et H Me CH.sub.2 OPr-i SO.sub.2 Me 125˜127 Me H Me CO.sub.2 CH.sub.2 CH.sub.2 OMe SO.sub.2 Me 114˜117 Et H Me CO.sub.2 CH.sub.2 CH.sub.2 OMe SO.sub.2 Me 122˜124 Me H Cl CH.sub.2 OCH.sub.2 CH.sub.2 OMe SO.sub.2 Me 157˜161 Et H Me CO.sub.2 Pr-n SO.sub.2 Me Oily Me H Cl CO.sub.2 Me SO.sub.2 Me 183˜185 Et H Cl CO.sub.2 Me SO.sub.2 Me 174˜176 i-Pr H Cl CO.sub.2 Me SO.sub.2 Me 138˜140 Me H OMe CO.sub.2 Me SO.sub.2 Me 195˜198 Me H Cl CO.sub.2 Pr-i SO.sub.2 Me 117˜119 Et H Cl CO.sub.2 Pr-i SO.sub.2 Me 141˜143 i-Pr H Me CO.sub.2 Me SO.sub.2 Me 116˜121 Me H OMe CH.sub.2 OMe SO.sub.2 Me 154˜157 Et H OMe CO.sub.2 Me SO.sub.2 Me 172˜175 Et H Cl CO.sub.2 Me Cl 167˜170 i-Pr H Cl CO.sub.2 Me Cl 144˜151 Et H Me CO.sub.2 Me SMe 142˜146 Et H Cl CH.sub.2 OMe Cl 102˜104 Et H Cl CO.sub.2 Et SO.sub.2 Me 100˜104 Et H Me CH.sub.2 OMe SMe Oily Me H Cl CH.sub.2 OMe Cl 141˜144 i-Pr H Cl CO.sub.2 Et SO.sub.2 Me 123˜126 Et H OMe CH.sub.2 OMe SO.sub.2 Me Oily Et H Me CHMeOEt SO.sub.2 Me Oily Et H Me CHEtOMe SO.sub.2 Me Oily Me H Cl OMe SO.sub.2 Me 229˜231 Et H Cl OMe SO.sub.2 Me 196˜198 Me H OMe H SO.sub.2 Me 202˜206 Et H Cl OPr SO.sub.2 Me 149˜151 Et H Cl OPr-i SO.sub.2 Me 142˜145 Et H Cl OEt SO.sub.2 Me 170˜174 Me H Cl OMe SO.sub.2 Me 229˜231 Et H Cl OMe SO.sub.2 Me 196˜198 Et H Me OMe SO.sub.2 Me 157˜159 i-Pr H Me OMe SO.sub.2 Me 135˜137 ______________________________________
Claims (34)
1. A substituted benzene of the formula I': ##STR23## selected from the group consisting of wherein: a) X is I, R1 is CN, R2 is H and R3 is SMe,
b) X is I, R1 is OMe, R2 is H and R3 is SMe,
c) X is Br, R1 is Cl, R2 is CO2 Me and R3 is SO2 Me,
d) X is Br, R1 is Cl, R2 is CO2 H and R3 is SO2 Me,
e) X is I, R1 is Cl, R2 is CO2 Me and R3 is SMe,
f) X is I, R1 is Cl, R2 is Co2 H and R3 is SMe,
g) X is I, R1 is Cl, R2 is CO2 Pr-i and R3 is SMe,
h) X is Br, R1 is Me, R2 is CO2 Me and R3 is SMe,
i) X is Br, R1 is Me, R2 CO2 H and R3 is SMe,
j) X is I, R1 is Me, R2 is CO2 Pr-i and R3 is SMe,
k) X is I, R1 is Me, R2 is CO2 Me and R3 is SMe,
l) X is I, R1 is Me, R2 is CO2 Me and R3 is SO2 Me,
m) X is I, R1 is Me, R2 is CO2 Et and R3 is SMe,
n) X is I, R1 is Me, R2 is CO2 Pr-i and R3 is SMe,
o) X is I, R1 is Me, R2 is CO2 CH2 CH2 OMe and R3 is SMe,
p) X is I, R1 is Me, R2 is CO2 CH2 CH2 Cl and R3 is SMe,
q) X is I, R1 is OMe, R2 is CO2 Me and R3 is SMe,
r) X is Br, R1 is Cl, R2 is CH2 OMe and R3 is SO2 Me,
s) X is I, R1 is Cl, R2 is CH2 OMe and R3 is SMe,
t) X is I, R1 is Me, R2 is CH2 OMe and R3 is SO2 Me,
u) X is I, R1 is Me, R2 is CH2 OMe and R3 is SMe,
v) X is I, R1 is Me, R2 is CH2 OEt and R3 is SMe,
w) X is I, R1 is Me, R2 is CH2 OPr-i and R3 is SMe,
x) X is I, R1 is OMe, R2 is CH2 OMe and R3 is SMe,
y) X is I, R1 is Me, R2 is CHMeOMe and R3 is SMe,
z) X is I, R1 is Me, R2 is CHMeOEt and R3 is SMe,
aa) X is I, R1 is Me, R2 is CHEtOMe and R3 is SMe,
bb) X is I, R1 is Me, R2 is OMe and R3 is SMe,
cc) X is I, R1 is Cl, R2 is Cl and R3 is SMe.
dd) X is I, R1 is Me, R2 is NO2 and R3 is SMe,
ee) X is Br, R1 is Cl, R2 is Me and R3 is SO2 Me,
ff) X is Br, R1 is Cl, R2 is Me and R3 is SMe,
gg) X is Br, R1 is Cl, R2 is CH2 OPr-i and R3 is SO2 Me.
2. A substituted benzene as defined in claim 1, wherein X is I, R1 is CN, R2 is H and R3 is SMe.
3. A substituted benzene as defined in claim 1, wherein X is I, R1 is OMe, R2 is H and R3 is SMe.
4. A substituted benzene as defined in claim 1, wherein X is Br, R1 is Cl, R2 is CO2 Me and R3 is SO2 Me.
5. A substituted benzene as defined in claim 1, wherein X is Br, R1 is Cl, R2 is CO2 H and R3 is SO2 Me.
6. A substituted benzene as defined in claim 1, wherein X is I, R1 is Cl, R2 is CO2 Me and R3 is SMe.
7. A substituted benzene as defined in claim 1, wherein X is I, R1 is Cl, R2 is CO2 H and R3 is SMe.
8. A substituted benzene as defined in claim 1, wherein X is I, R1 is Cl, R2 is CO2 Pr-i and R3 is SMe.
9. A substituted benzene as defined in claim 1, wherein X is Br, R1 is Me, R2 is CO2 Me and R3 is SMe.
10. A substituted benzene as defined in claim 1, wherein X is Br, R1 is Me, R2 is CO2 H and R3 is SMe.
11. A substituted benzene as defined in claim 1, wherein X is Br, R1 is Me, R2 is CO2 H and R3 is SMe.
12. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CO2 Me and R3 is SMe.
13. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CO2 Me and R3 is SO2 Me.
14. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CO2 Et and R3 is SMe.
15. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CO2 Pr-i and R3 is SMe.
16. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CO2 CH2 CH2 OMe and R3 is SMe.
17. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CO2 CH2 CH2 Cl and R3 is SMe.
18. A substituted benzene as defined in claim 1, wherein X is I, R1 is OMe, R2 is CO2 Me and R3 is SMe.
19. A substituted benzene as defined in claim 1, wherein X is Br, R1 is Cl, R2 is CH2 OMe and R3 is SO2 Me.
20. A substituted benzene as defined in claim 1, wherein X is I, R1 is Cl, R2 is CH2 OMe and R3 is SMe.
21. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CH2 OMe and R3 is SO2 Me.
22. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CH2 OMe and R3 is SMe.
23. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CH2 OEt and R3 is SMe.
24. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CH2 OPr-i and R3 is SMe.
25. A substituted benzene as defined in claim 1, wherein X is I, R1 is OMe, R2 is CH2 OMe and R3 is SMe.
26. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CHMeOMe and R3 is SMe.
27. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CHMeOEt and R3 is SMe.
28. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is CHEtOMe and R3 is SMe.
29. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is OMe and R3 is SMe.
30. A substituted benzene as defined in claim 1, wherein X is I, R1 is Cl, R2 is Cl and R3 is SMe.
31. A substituted benzene as defined in claim 1, wherein X is I, R1 is Me, R2 is NO2 and R3 is SMe.
32. A substituted benzene as defined in claim 1, wherein X is Br, R1 is Cl, R2 is Me and R3 is SO2 Me.
33. A substituted benzene as defined in claim 1, wherein X is Br, R1 is Cl, R2 is Me and R3 is SMe.
34. A substituted benzene as defined in claim 1, wherein X is Br, R1 is Cl, R2 is CH2 OPr-i and R3 is SO2 Me.
Priority Applications (1)
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US07/885,989 USRE34423E (en) | 1988-06-03 | 1992-05-20 | Substituted benzenes useful as intermediates |
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JP63-137095 | 1988-06-03 | ||
JP13709588 | 1988-06-03 | ||
JP1098284A JPH02237978A (en) | 1988-06-03 | 1989-04-18 | Production of 4-benzoyl-5-hydroxypyrazole |
JP1-98284 | 1989-04-18 | ||
US07/360,468 US4942246A (en) | 1988-06-03 | 1989-06-02 | Process for producing 4-benzoyl-5-hydroxypyrazoles |
US07/519,727 US5087724A (en) | 1988-06-03 | 1990-05-07 | Substituted benzenes useful as intermediates |
US07/885,989 USRE34423E (en) | 1988-06-03 | 1992-05-20 | Substituted benzenes useful as intermediates |
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US07/360,468 Division US4942246A (en) | 1988-06-03 | 1989-06-02 | Process for producing 4-benzoyl-5-hydroxypyrazoles |
US07/519,727 Reissue US5087724A (en) | 1988-06-03 | 1990-05-07 | Substituted benzenes useful as intermediates |
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Cited By (1)
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---|---|---|---|---|
WO1998042677A1 (en) * | 1997-03-24 | 1998-10-01 | Dow Agrosciences Llc | Process for preparing 1-alkyl-4- (2-chloro-3-alkoxy-4-alkylsulfonylbenzoyl) -5-hydroxypyrazole and related compounds |
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