SK286835B6 - Spôsob prípravy 5- a/alebo 6-substituovaných esterov kyseliny hydroxybenzoovej - Google Patents
Spôsob prípravy 5- a/alebo 6-substituovaných esterov kyseliny hydroxybenzoovej Download PDFInfo
- Publication number
- SK286835B6 SK286835B6 SK68-2002A SK682002A SK286835B6 SK 286835 B6 SK286835 B6 SK 286835B6 SK 682002 A SK682002 A SK 682002A SK 286835 B6 SK286835 B6 SK 286835B6
- Authority
- SK
- Slovakia
- Prior art keywords
- formula
- compound
- alkyl
- preparation
- solvent
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 33
- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- -1 6-substituted-2- hydroxybenzoic acid esters Chemical class 0.000 title claims description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 34
- 239000002904 solvent Substances 0.000 claims abstract description 15
- 239000012965 benzophenone Substances 0.000 claims abstract description 6
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 6
- 125000005843 halogen group Chemical group 0.000 claims abstract description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 7
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical group [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 6
- 230000000855 fungicidal effect Effects 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001632 sodium acetate Substances 0.000 claims description 4
- 235000017281 sodium acetate Nutrition 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 abstract description 9
- 230000015572 biosynthetic process Effects 0.000 abstract description 8
- 238000004519 manufacturing process Methods 0.000 abstract description 7
- 229930014626 natural product Natural products 0.000 abstract description 5
- 239000007858 starting material Substances 0.000 abstract description 5
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000417 fungicide Substances 0.000 abstract description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 150000001734 carboxylic acid salts Chemical class 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 239000000047 product Substances 0.000 description 8
- 229960000583 acetic acid Drugs 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000005481 NMR spectroscopy Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- 150000001299 aldehydes Chemical class 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- KCLNHRSLECZYEW-UHFFFAOYSA-N ethyl 2-acetyloxy-3-oxobutanoate Chemical compound CCOC(=O)C(C(C)=O)OC(C)=O KCLNHRSLECZYEW-UHFFFAOYSA-N 0.000 description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- 150000005166 2-hydroxybenzoic acids Chemical class 0.000 description 2
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 229940040526 anhydrous sodium acetate Drugs 0.000 description 2
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 2
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 2
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 2
- RDULEYWUGKOCMR-UHFFFAOYSA-N ethyl 2-chloro-3-oxobutanoate Chemical compound CCOC(=O)C(Cl)C(C)=O RDULEYWUGKOCMR-UHFFFAOYSA-N 0.000 description 2
- KWXBNUYCDMPLEQ-UHFFFAOYSA-N ethyl 2-hydroxy-6-methylbenzoate Chemical compound CCOC(=O)C1=C(C)C=CC=C1O KWXBNUYCDMPLEQ-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 239000003586 protic polar solvent Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- 239000012258 stirred mixture Substances 0.000 description 2
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
- QHMYICVZNHGMPP-UHFFFAOYSA-N 2-acetyloxy-3-oxobutanoic acid Chemical compound CC(=O)OC(C(C)=O)C(O)=O QHMYICVZNHGMPP-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 101000939500 Homo sapiens UBX domain-containing protein 11 Proteins 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 102100029645 UBX domain-containing protein 11 Human genes 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 230000002552 anti-phytopathogenic effect Effects 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000012320 chlorinating reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000013375 chromatographic separation Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- ZGYXABNSOOACGL-UHFFFAOYSA-N ethyl 2-hydroxy-5-methylbenzoate Chemical compound CCOC(=O)C1=CC(C)=CC=C1O ZGYXABNSOOACGL-UHFFFAOYSA-N 0.000 description 1
- OHLRLMWUFVDREV-UHFFFAOYSA-N ethyl 4-chloro-3-oxobutanoate Chemical compound CCOC(=O)CC(=O)CCl OHLRLMWUFVDREV-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/46—Friedel-Crafts reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35403799A | 1999-07-15 | 1999-07-15 | |
| PCT/US2000/018768 WO2001005739A1 (en) | 1999-07-15 | 2000-07-10 | Process for the preparation of 5- and/or 6-substituted-2-hydroxybenzoic acid esters |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK682002A3 SK682002A3 (en) | 2002-08-06 |
| SK286835B6 true SK286835B6 (sk) | 2009-06-05 |
Family
ID=23391634
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK68-2002A SK286835B6 (sk) | 1999-07-15 | 2000-07-10 | Spôsob prípravy 5- a/alebo 6-substituovaných esterov kyseliny hydroxybenzoovej |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US6441219B1 (cs) |
| EP (1) | EP1196370B1 (cs) |
| JP (1) | JP3779615B2 (cs) |
| KR (1) | KR100651090B1 (cs) |
| CN (1) | CN1160304C (cs) |
| AT (1) | ATE249415T1 (cs) |
| AU (1) | AU5926300A (cs) |
| BR (1) | BR0012493B1 (cs) |
| CA (1) | CA2379342C (cs) |
| CZ (1) | CZ300511B6 (cs) |
| DE (1) | DE60005193T2 (cs) |
| DK (1) | DK1196370T3 (cs) |
| ES (1) | ES2207528T3 (cs) |
| HU (1) | HU229906B1 (cs) |
| IL (2) | IL147027A0 (cs) |
| MX (1) | MXPA02000395A (cs) |
| RU (1) | RU2245325C2 (cs) |
| SK (1) | SK286835B6 (cs) |
| WO (1) | WO2001005739A1 (cs) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002051790A1 (en) * | 2000-12-23 | 2002-07-04 | Basf Aktiengesellschaft | Process for the preparation of 5- and/or 6 - substituted - 2 - hydroxy-benzoic acid esters |
| US6559336B2 (en) * | 1999-07-15 | 2003-05-06 | Basf Aktiengesellschaft | Process for the preparation of 5- and/or 6-substituted-2-hydroxybenzoic acid esters |
| AU2013209719A1 (en) | 2012-01-18 | 2014-08-07 | Zafgen, Inc. | Tricyclic sulfone compounds and methods of making and using same |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2107958C3 (de) | 1971-02-19 | 1980-08-21 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von a -Naphtholen |
| US5773663A (en) * | 1996-05-01 | 1998-06-30 | American Cyanamid Company | Fungicidal methods, compounds and compositions containing benzophenones |
| US5945567A (en) | 1997-08-20 | 1999-08-31 | American Cyanamid Company | Fungicidal 2-methoxybenzophenones |
-
2000
- 2000-07-10 DK DK00945295T patent/DK1196370T3/da active
- 2000-07-10 ES ES00945295T patent/ES2207528T3/es not_active Expired - Lifetime
- 2000-07-10 AU AU59263/00A patent/AU5926300A/en not_active Abandoned
- 2000-07-10 SK SK68-2002A patent/SK286835B6/sk not_active IP Right Cessation
- 2000-07-10 CN CNB008101779A patent/CN1160304C/zh not_active Expired - Lifetime
- 2000-07-10 MX MXPA02000395A patent/MXPA02000395A/es active IP Right Grant
- 2000-07-10 CZ CZ20020112A patent/CZ300511B6/cs not_active IP Right Cessation
- 2000-07-10 HU HU0202331A patent/HU229906B1/hu not_active IP Right Cessation
- 2000-07-10 CA CA002379342A patent/CA2379342C/en not_active Expired - Fee Related
- 2000-07-10 AT AT00945295T patent/ATE249415T1/de active
- 2000-07-10 EP EP00945295A patent/EP1196370B1/en not_active Expired - Lifetime
- 2000-07-10 BR BRPI0012493-1A patent/BR0012493B1/pt not_active IP Right Cessation
- 2000-07-10 RU RU2002102233/04A patent/RU2245325C2/ru not_active IP Right Cessation
- 2000-07-10 IL IL14702700A patent/IL147027A0/xx active IP Right Grant
- 2000-07-10 KR KR1020027000513A patent/KR100651090B1/ko not_active Expired - Fee Related
- 2000-07-10 WO PCT/US2000/018768 patent/WO2001005739A1/en active IP Right Grant
- 2000-07-10 JP JP2001511400A patent/JP3779615B2/ja not_active Expired - Fee Related
- 2000-07-10 DE DE60005193T patent/DE60005193T2/de not_active Expired - Lifetime
- 2000-10-30 US US09/699,775 patent/US6441219B1/en not_active Expired - Lifetime
-
2001
- 2001-12-11 IL IL147027A patent/IL147027A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR100651090B1 (ko) | 2006-11-29 |
| HUP0202331A2 (hu) | 2002-11-28 |
| JP2003505355A (ja) | 2003-02-12 |
| IL147027A0 (en) | 2002-08-14 |
| WO2001005739A1 (en) | 2001-01-25 |
| CZ2002112A3 (cs) | 2002-05-15 |
| DK1196370T3 (da) | 2004-01-12 |
| ES2207528T3 (es) | 2004-06-01 |
| BR0012493B1 (pt) | 2011-02-22 |
| KR20020012629A (ko) | 2002-02-16 |
| EP1196370A1 (en) | 2002-04-17 |
| JP3779615B2 (ja) | 2006-05-31 |
| SK682002A3 (en) | 2002-08-06 |
| CN1360564A (zh) | 2002-07-24 |
| DE60005193D1 (de) | 2003-10-16 |
| HUP0202331A3 (en) | 2005-01-28 |
| HU229906B1 (en) | 2014-12-29 |
| CZ300511B6 (cs) | 2009-06-03 |
| CN1160304C (zh) | 2004-08-04 |
| BR0012493A (pt) | 2002-04-02 |
| CA2379342A1 (en) | 2001-01-25 |
| RU2245325C2 (ru) | 2005-01-27 |
| IL147027A (en) | 2006-12-31 |
| MXPA02000395A (es) | 2002-07-02 |
| US6441219B1 (en) | 2002-08-27 |
| CA2379342C (en) | 2007-01-02 |
| ATE249415T1 (de) | 2003-09-15 |
| AU5926300A (en) | 2001-02-05 |
| EP1196370B1 (en) | 2003-09-10 |
| DE60005193T2 (de) | 2004-07-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Patent lapsed due to non-payment of maintenance fees |
Effective date: 20140710 |