PL85122B1 - - Google Patents
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- Publication number
- PL85122B1 PL85122B1 PL1972159123A PL15912372A PL85122B1 PL 85122 B1 PL85122 B1 PL 85122B1 PL 1972159123 A PL1972159123 A PL 1972159123A PL 15912372 A PL15912372 A PL 15912372A PL 85122 B1 PL85122 B1 PL 85122B1
- Authority
- PL
- Poland
- Prior art keywords
- alkoxy
- alkyl
- reacted
- oxidation
- oxidizing agent
- Prior art date
Links
- 239000002253 acid Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000007800 oxidant agent Substances 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 4
- -1 alkyl sulphate Chemical compound 0.000 claims description 4
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 claims description 4
- 239000012286 potassium permanganate Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 150000001350 alkyl halides Chemical class 0.000 claims description 3
- 229940100198 alkylating agent Drugs 0.000 claims description 3
- 239000002168 alkylating agent Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims 3
- 238000007254 oxidation reaction Methods 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- 229910021653 sulphate ion Inorganic materials 0.000 claims 2
- 230000029936 alkylation Effects 0.000 claims 1
- 238000005804 alkylation reaction Methods 0.000 claims 1
- 230000031709 bromination Effects 0.000 claims 1
- 238000005893 bromination reaction Methods 0.000 claims 1
- 229930003836 cresol Natural products 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- DTFKRVXLBCAIOZ-UHFFFAOYSA-N 2-methylanisole Chemical compound COC1=CC=CC=C1C DTFKRVXLBCAIOZ-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- BXWLVQXAFBWKSR-UHFFFAOYSA-N 2-methoxy-5-methylsulfonylbenzoic acid Chemical compound COC1=CC=C(S(C)(=O)=O)C=C1C(O)=O BXWLVQXAFBWKSR-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C315/00—Preparation of sulfones; Preparation of sulfoxides
- C07C315/02—Preparation of sulfones; Preparation of sulfoxides by formation of sulfone or sulfoxide groups by oxidation of sulfides, or by formation of sulfone groups by oxidation of sulfoxides
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Description
Przedmiotem wynalazku jest sposób wytwarza¬ nia kwasu 2-alkoksy-5-aljkilosuLfonylobenzoasowego o wzorze 1, w którym X i Y oznaczaja rodnik alki¬ lowy lub alkenilowy o 1—4 atomach wegla.Te pochodne kwasu benzoesowego stanowia cen¬ ny produlkt posredni przy wytwarzaniu aktywnych substancji biologicznie czynnych, stosowany zwla¬ szcza w przemysle farmaceutycznym, szczególnie jako srodek leczniczy zarówno gastro-enterologii i neurologii jak i w innych dziedzinach.Sposób wytwarzania kwasu benzoesowego we¬ dlug wynalazku polega na tym, ze o-krezol pod¬ daje sie alkilowaniu srodkiem alkilujacym, takim jatk siarczan alkilowy, halogenek alkilowy lub siar¬ czan alkiloarylowy i wytworzony o-alkokisykreozol bromuje sie do 2alkofesy-'5Hbromotoluenu, a na¬ stepnie poddaije sie reakcji z merkaptydem, otrzy¬ mujac 2-aJikoksy-5-aLlkilotio-toluen, który nastep¬ nie poddaje sie utlenianiu srodkiem utleniajacym, takim jak nadmanganian potasu i otrzymuje kwas 2alkoksy-5-alkilosulfonylobenzoesowy.Wariant sposobu wedlug wynalazku polega na tym, ze 2-alkokisy-5-alki]otiotoluen najpierw pod¬ daje sie utlenianiu srodkiem utleniajacym, takim jak nadtlenek wodoru lub dwuchromian potasowy do 2-alkoksyH5-alkilosulfonyloto(luenu, który naste¬ pnie utlenia sie dalszym srodkiem utleniajacym taMm, jak nadmanganian potasu otrzymujac kwas 2-alkoksy-5-aJkilosuMonyilobenzoesowy.Proces wedlug wynalazku przebiega wedlug sche- 2 matu przedstawionego na rysunku, gdzie zwiazek o wzorze Y—S—Me oznacza merkaptyd, z tym, ze Me oznacza metal, a Y reszte organiczna.Sposób wytwarzania dwóch pochodnych kwasu 8 benzoesowego opisano w nastepujacych przykla¬ dach: Przyklad I. Kwas 2-nnetoksy-5-metylosulfo- nylobenzoesowy. io o-metoksytoluen. Do naczynia reakcyjnego o po¬ jemnosci 4 litrów zaopatrzonego w chlodnice, ter¬ mometr i wkraplaez wprowadza sie 324 gramów o-fcrozoliu, 300 mililitrów wody i 300 mililitrów lu¬ gu sodowego, po czym wkrapla sie stopniowo 378 gramów siarczanu dwumetylowego w temperaturze °C i ogrzewa przez 10 minut pod chlodnica zwrotna. Po ochlodzeniu dodaje sie dalsze 75 mili¬ litrów lugu sodowego i 189 gramów siarczanu dwu- imetylowego, po czyim ogrzewa przez 15 minut pod chlodnica zwrotna. Nastepnie roztwór ochladza sie, dodaje 90 mililitrów lugu sodowego i ogrzewa pod chlodnica zwrotna przez 4 godziny. Po ochlodze¬ niu produkt rozciencza sie, dodajac 700 mililitrów wody i dekantuje warstwe oleista. Warstwe wodna » ekstrahuje sie trzykrotnie 300 mililitrami chlorku metylenu. Oddzielona warstwe oleista i ekstrakty chlorku etylenu suszy sie razem nad siarczanem sodowym. Nastepnie rozpuszczalnik odparowuje sie pod obnizanym cisnieniem i destyluje pozostalosc 80 oleista. 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Claims (2)
- Zastrzezenia patentowe 1. Sposób wytwarzania kwasu 2-alkoksy-5-alki- lasulfonylobenizoesowego o wzorze ogólnym 1, w którymi X i Y oznaczaja rodniki alkilowe lub alkenylowe o 1—4 atomacji wegla, znamienny tym, ze onkrezol poddaje sie alkilowaniu srodkiem alki¬ lujacyim, takim jak siarczan alkilowy, halogenek alkilowy lub siarczan alkiloarylowy i wytworzony o-alkoksykrezol bromuje sie do 2-alkokisy-5-bromo- toluenu, który nastepnie poddaje sie reakcji z mer- kaptydem, otrzymujac 2^aflfcoksy-5-alkilotiotoluen, który nastepnie poddaje sie utlenianiu srodkiem utleniajacym takim jak nadmanganian potasu.
- 2. Sposób wytwarzania kwasu 2-alkoksy-5-alki- 10 15 losulfonylobenzoesowego o wzorze ogólnym 1, w którym X i Y oznaczaja rodniki alkilowe lub alkenylowe o 1—4 atomach wegla, znamienny tym, ze onkrezol poddaje sie alkilowaniu srodkiem alki¬ lujacym, takim jak siarczan alkilowy, halogenek alkilowy lub siarczan alkiloarylowy i wytworzony o-alkoksykrezol bromuje sie do 2-alkoksy-5-bro- motoluenu, który nastepnie poddaje sie reakcji z merkaptydem i otrzymany 2-alkoksy-5-alkilotio- toluen poddaje sie najpierw utlenieniu srodkiem utleniajacym, takim jak nadtlenek wodoru lub dwuchromian potasowy do 2-alkoksy-5-alkilosulfo- nylotoluenu, który nasetpnie utlenia sie za pomoca dalszego srodka utleniajacego, takiego jak nad¬ manganian potasu. Y-SO, C00H 0-X klxór iCH5 CH, OH .... . ^-^0-X alkilowanie _ CH3 CH3 bromowanie Br CH, CH5 y '3 0-X_^_s-Me^ -^0-X Y-sr CH, COOH Y-S o-x utlenienie Y-CLS o-x Schemat DN-3 zam. 2538/76 Cena 10 zl PL
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1080372A CH565758A5 (pl) | 1972-07-19 | 1972-07-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL85122B1 true PL85122B1 (pl) | 1976-04-30 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1972159123A PL85122B1 (pl) | 1972-07-19 | 1972-11-27 |
Country Status (31)
| Country | Link |
|---|---|
| US (1) | US3878240A (pl) |
| JP (2) | JPS4935356A (pl) |
| AR (1) | AR192695A1 (pl) |
| AT (1) | AT321891B (pl) |
| AU (1) | AU469248B2 (pl) |
| BE (1) | BE793689A (pl) |
| BG (1) | BG20097A3 (pl) |
| CA (1) | CA993885A (pl) |
| CH (1) | CH565758A5 (pl) |
| CS (1) | CS181716B2 (pl) |
| DD (1) | DD101665A5 (pl) |
| DE (1) | DE2259239A1 (pl) |
| EG (1) | EG11125A (pl) |
| ES (1) | ES409349A1 (pl) |
| FR (1) | FR2163301A5 (pl) |
| GB (1) | GB1364404A (pl) |
| HU (1) | HU174964B (pl) |
| IE (1) | IE37364B1 (pl) |
| IL (1) | IL41380A (pl) |
| IT (1) | IT1048404B (pl) |
| LU (1) | LU66805A1 (pl) |
| MC (1) | MC960A1 (pl) |
| NL (1) | NL7216405A (pl) |
| NO (1) | NO138947C (pl) |
| OA (1) | OA04328A (pl) |
| PL (1) | PL85122B1 (pl) |
| RO (1) | RO62849A (pl) |
| SE (1) | SE402454B (pl) |
| YU (1) | YU36496B (pl) |
| ZA (1) | ZA73142B (pl) |
| ZM (1) | ZM1073A1 (pl) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4609712A (en) * | 1984-06-18 | 1986-09-02 | General Electric Company | Method for preparing monomeric and polymeric bis(dicarboxyphenyl) sulfone compounds |
| US4625013A (en) * | 1984-12-20 | 1986-11-25 | General Electric Company | Aromatic sulfoxy compositions and method for their preparation |
| US4898973A (en) * | 1985-03-07 | 1990-02-06 | Ici Americas Inc. | Trisubstituted benzoic acid intermediates |
| GB9310699D0 (en) * | 1993-05-24 | 1993-07-07 | Zeneca Ltd | Chemical process |
| KR100809489B1 (ko) * | 2001-10-10 | 2008-03-03 | 씨제이제일제당 (주) | 사이클로옥시게나제-2의 저해제로서 선택성이 뛰어난4'-메탄설포닐-비페닐 유도체 |
| AU2003286183A1 (en) * | 2002-12-23 | 2004-07-22 | Dsm Fine Chemicals Austria Nfg Gmbh And Co Kg | Method for producing optionally substituted benzoic acids |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3342826A (en) * | 1964-01-13 | 1967-09-19 | Ile De France | Heterocyclic aminoalkyl benzamides |
| NL7008629A (pl) * | 1969-06-25 | 1970-12-29 | ||
| NL7008630A (pl) * | 1969-06-25 | 1970-12-29 |
-
0
- BE BE793689D patent/BE793689A/xx not_active IP Right Cessation
-
1972
- 1972-07-19 CH CH1080372A patent/CH565758A5/xx not_active IP Right Cessation
- 1972-11-22 SE SE7215174A patent/SE402454B/xx unknown
- 1972-11-22 NO NO4265/72A patent/NO138947C/no unknown
- 1972-11-27 PL PL1972159123A patent/PL85122B1/pl unknown
- 1972-11-30 BG BG022006A patent/BG20097A3/xx unknown
- 1972-11-30 HU HU72RE522A patent/HU174964B/hu unknown
- 1972-12-01 NL NL7216405A patent/NL7216405A/xx unknown
- 1972-12-04 DE DE2259239A patent/DE2259239A1/de active Pending
- 1972-12-05 YU YU03014/72A patent/YU36496B/xx unknown
- 1972-12-06 CS CS7200008354A patent/CS181716B2/cs unknown
- 1972-12-06 ES ES409349A patent/ES409349A1/es not_active Expired
- 1972-12-08 RO RO7200073084A patent/RO62849A/ro unknown
- 1972-12-12 AR AR245595A patent/AR192695A1/es active
- 1972-12-13 AT AT1061872A patent/AT321891B/de not_active IP Right Cessation
- 1972-12-18 US US315842A patent/US3878240A/en not_active Expired - Lifetime
- 1972-12-29 FR FR7246873A patent/FR2163301A5/fr not_active Expired
-
1973
- 1973-01-08 ZA ZA730142A patent/ZA73142B/xx unknown
- 1973-01-08 AU AU50863/73A patent/AU469248B2/en not_active Expired
- 1973-01-09 LU LU66805A patent/LU66805A1/xx unknown
- 1973-01-09 CA CA160,847A patent/CA993885A/en not_active Expired
- 1973-01-18 DD DD168316A patent/DD101665A5/xx unknown
- 1973-01-24 IL IL41380A patent/IL41380A/en unknown
- 1973-01-25 ZM ZM10/73A patent/ZM1073A1/xx unknown
- 1973-01-30 MC MC1028A patent/MC960A1/fr unknown
- 1973-02-02 OA OA54822A patent/OA04328A/xx unknown
- 1973-02-06 JP JP48014355A patent/JPS4935356A/ja active Pending
- 1973-02-21 GB GB846773A patent/GB1364404A/en not_active Expired
- 1973-02-28 IT IT7320973A patent/IT1048404B/it active
- 1973-03-02 IE IE340/73A patent/IE37364B1/xx unknown
- 1973-04-03 JP JP48037497A patent/JPS5222B2/ja not_active Expired
- 1973-07-15 EG EG276/73A patent/EG11125A/xx active
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