DE68903120T2 - Verfahren zur herstellung von zyklischen sulfaten. - Google Patents
Verfahren zur herstellung von zyklischen sulfaten.Info
- Publication number
- DE68903120T2 DE68903120T2 DE8989400619T DE68903120T DE68903120T2 DE 68903120 T2 DE68903120 T2 DE 68903120T2 DE 8989400619 T DE8989400619 T DE 8989400619T DE 68903120 T DE68903120 T DE 68903120T DE 68903120 T2 DE68903120 T2 DE 68903120T2
- Authority
- DE
- Germany
- Prior art keywords
- radicals
- sulfate
- process according
- alkyl
- cyclic
- 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 - Fee Related
Links
- 238000000034 method Methods 0.000 title claims description 16
- 238000004519 manufacturing process Methods 0.000 title claims 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 title 1
- -1 alkoxycarbonyl radical Chemical class 0.000 claims description 25
- 239000005708 Sodium hypochlorite Substances 0.000 claims description 11
- WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 claims description 11
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical group [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 7
- 125000004122 cyclic group Chemical group 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004104 aryloxy group Chemical group 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 230000003647 oxidation Effects 0.000 claims description 5
- 238000007254 oxidation reaction Methods 0.000 claims description 5
- 150000003304 ruthenium compounds Chemical class 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- YBCAZPLXEGKKFM-UHFFFAOYSA-K ruthenium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Ru+3] YBCAZPLXEGKKFM-UHFFFAOYSA-K 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- SUEZQPIECXNOJE-UHFFFAOYSA-N 4-(chloromethyl)-1,3,2-dioxathiolane 2,2-dioxide Chemical compound ClCC1COS(=O)(=O)O1 SUEZQPIECXNOJE-UHFFFAOYSA-N 0.000 claims description 2
- OQXNUCOGMMHHNA-UHFFFAOYSA-N 4-methyl-1,3,2-dioxathiolane 2,2-dioxide Chemical compound CC1COS(=O)(=O)O1 OQXNUCOGMMHHNA-UHFFFAOYSA-N 0.000 claims description 2
- ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 150000008282 halocarbons Chemical class 0.000 claims 1
- SATVIFGJTRRDQU-UHFFFAOYSA-N potassium hypochlorite Chemical compound [K+].Cl[O-] SATVIFGJTRRDQU-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 24
- 238000003756 stirring Methods 0.000 description 13
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 239000012074 organic phase Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 5
- GSAWJDWGUUYIPS-UHFFFAOYSA-N O.O.[Ru]=O Chemical compound O.O.[Ru]=O GSAWJDWGUUYIPS-UHFFFAOYSA-N 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 229910001925 ruthenium oxide Inorganic materials 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- GJFJJZHAMZHQMO-UHFFFAOYSA-N dioxoruthenium dihydrate Chemical compound O.O.O=[Ru]=O GJFJJZHAMZHQMO-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 3
- 238000002329 infrared spectrum Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- ZTWIEIFKPFJRLV-UHFFFAOYSA-K trichlororuthenium;trihydrate Chemical compound O.O.O.Cl[Ru](Cl)Cl ZTWIEIFKPFJRLV-UHFFFAOYSA-K 0.000 description 3
- WDXYVJKNSMILOQ-UHFFFAOYSA-N 1,3,2-dioxathiolane 2-oxide Chemical compound O=S1OCCO1 WDXYVJKNSMILOQ-UHFFFAOYSA-N 0.000 description 2
- SAPINXZHMGNTEC-UHFFFAOYSA-N 4,5-dimethyl-1,3,2-dioxathiolane 2-oxide Chemical compound CC1OS(=O)OC1C SAPINXZHMGNTEC-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- LIUXPCWTAWPQPM-UHFFFAOYSA-N 4,4,5,5-tetramethyl-1,3,2-dioxathiolane 2,2-dioxide Chemical compound CC1(C)OS(=O)(=O)OC1(C)C LIUXPCWTAWPQPM-UHFFFAOYSA-N 0.000 description 1
- SVOJBLJQIJSBJC-UHFFFAOYSA-N 4,4,5,5-tetramethyl-1,3,2-dioxathiolane 2-oxide Chemical compound CC1(C)OS(=O)OC1(C)C SVOJBLJQIJSBJC-UHFFFAOYSA-N 0.000 description 1
- POVNYOLUWDFQOZ-UHFFFAOYSA-N 4,5-dimethyl-1,3,2-dioxathiolane 2,2-dioxide Chemical compound CC1OS(=O)(=O)OC1C POVNYOLUWDFQOZ-UHFFFAOYSA-N 0.000 description 1
- RGDJXHLNJJZNGO-UHFFFAOYSA-N 4-(chloromethyl)-1,3,2-dioxathiolane 2-oxide Chemical compound ClCC1COS(=O)O1 RGDJXHLNJJZNGO-UHFFFAOYSA-N 0.000 description 1
- SJHAYVFVKRXMKG-UHFFFAOYSA-N 4-methyl-1,3,2-dioxathiolane 2-oxide Chemical compound CC1COS(=O)O1 SJHAYVFVKRXMKG-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 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
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 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
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- CUILPNURFADTPE-UHFFFAOYSA-N hypobromous acid Chemical class BrO CUILPNURFADTPE-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003303 ruthenium Chemical class 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/10—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms two oxygen atoms and one sulfur atom, e.g. cyclic sulfates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Epoxy Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8802917A FR2628423B1 (fr) | 1988-03-08 | 1988-03-08 | Procede de preparation de sulfates cycliques |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE68903120D1 DE68903120D1 (de) | 1992-11-12 |
| DE68903120T2 true DE68903120T2 (de) | 1993-04-15 |
Family
ID=9364007
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE8989400619T Expired - Fee Related DE68903120T2 (de) | 1988-03-08 | 1989-03-06 | Verfahren zur herstellung von zyklischen sulfaten. |
Country Status (24)
| Country | Link |
|---|---|
| US (2) | US4960904A (en:Method) |
| EP (1) | EP0332521B1 (en:Method) |
| JP (1) | JPH0285276A (en:Method) |
| KR (1) | KR910003712B1 (en:Method) |
| CN (1) | CN1025498C (en:Method) |
| AR (1) | AR244678A1 (en:Method) |
| AT (1) | ATE81339T1 (en:Method) |
| AU (1) | AU617768B2 (en:Method) |
| CA (1) | CA1322375C (en:Method) |
| DE (1) | DE68903120T2 (en:Method) |
| DK (1) | DK110289A (en:Method) |
| ES (1) | ES2045481T3 (en:Method) |
| FI (1) | FI92484C (en:Method) |
| FR (1) | FR2628423B1 (en:Method) |
| GR (1) | GR3005893T3 (en:Method) |
| HU (1) | HU201750B (en:Method) |
| IE (1) | IE890717L (en:Method) |
| IL (1) | IL89518A (en:Method) |
| MX (1) | MX169507B (en:Method) |
| NO (1) | NO171678C (en:Method) |
| PT (1) | PT89946B (en:Method) |
| SU (1) | SU1720488A3 (en:Method) |
| YU (1) | YU46890B (en:Method) |
| ZA (1) | ZA891693B (en:Method) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2631340B1 (fr) * | 1988-05-16 | 1990-07-27 | Rhone Poulenc Sante | Procede de preparation de sulfates cycliques |
| US5159100A (en) * | 1990-12-19 | 1992-10-27 | Lonza Ltd. | Process for the production of cyclopropanenitrile derivatives |
| US5189200A (en) * | 1990-12-21 | 1993-02-23 | Sepracor, Inc. | Process for the stereoselective transformation of a diol to an alcohol |
| FR2676736B1 (fr) * | 1991-05-23 | 1993-08-06 | Rhone Poulenc Rorer Sa | Nouveaux sulfates chiraux, leur preparation et leur emploi dans la synthese de produits pharmaceutiques. |
| US5171892A (en) * | 1991-07-02 | 1992-12-15 | E. I. Du Pont De Nemours And Company | Chiral phospholanes via chiral 1,4-diol cyclic sulfates |
| US5336683A (en) * | 1992-01-24 | 1994-08-09 | Hoffmann-La Roche Inc. | Antioxidants |
| US6180799B1 (en) * | 2000-05-01 | 2001-01-30 | The United States Of America As Represented By The Secretary Of The Air Force | Sulfalation of tetraol |
| CN101293887A (zh) * | 2007-04-26 | 2008-10-29 | 中国科学院福建物质结构研究所 | 一种高纯度环状硫酸酯的纯化方法 |
| CN101456857B (zh) * | 2007-12-11 | 2014-03-05 | 中国科学院福建物质结构研究所 | 一种制备高纯度环状硫酸酯的方法 |
| CN101870688A (zh) * | 2009-04-24 | 2010-10-27 | 中国科学院福建物质结构研究所 | 一种4-甲基硫酸亚乙酯的合成方法 |
| CN104945368B (zh) * | 2015-05-29 | 2018-06-01 | 石家庄圣泰化工有限公司 | 一种生产4-丙基硫酸乙烯酯的方法 |
| CN106905291A (zh) * | 2015-12-22 | 2017-06-30 | 天津鑫源广泰新材料科技有限公司 | 一种3，3—联二硫酸乙烯酯的生产方法 |
| CN106187989B (zh) * | 2016-07-26 | 2018-11-23 | 张家港瀚康化工有限公司 | 硫酸乙烯酯的制备方法 |
| CN109422719A (zh) * | 2017-08-30 | 2019-03-05 | 张家港市国泰华荣化工新材料有限公司 | 环状硫酸酯的制备方法 |
| CN109485632B (zh) * | 2017-09-13 | 2021-05-07 | 山东石大胜华化工集团股份有限公司 | 环状亚硫酸酯的制备方法 |
| CN107973774B (zh) * | 2017-11-13 | 2020-07-17 | 张家港瀚康化工有限公司 | 利用微通道反应器制备硫酸乙烯酯的方法 |
| KR102080198B1 (ko) * | 2018-08-22 | 2020-04-07 | 주식회사 알이피 | 차아염소산 칼슘을 이용한 산화방법 및 설폰 또는 설페이트 화합물을 제조하는 방법 |
| CN111825652A (zh) * | 2019-04-17 | 2020-10-27 | 江苏长园华盛新能源材料有限公司 | 制备硫酸乙烯酯的方法 |
| CN111662268B (zh) * | 2020-06-12 | 2023-01-10 | 上海如鲲新材料股份有限公司 | 一种环状硫酸酯类化合物的制备方法及其应用 |
| KR102355699B1 (ko) * | 2020-10-27 | 2022-02-07 | 솔브레인 주식회사 | 유기 황 화합물의 제조방법 |
| KR20220057819A (ko) * | 2020-10-30 | 2022-05-09 | 솔브레인 주식회사 | 유기 황 화합물의 인시츄 제조방법 |
| CN112679466A (zh) * | 2020-12-27 | 2021-04-20 | 江苏瀚康新材料有限公司 | 一种硫酸乙烯酯的合成方法 |
| CN116764678B (zh) * | 2022-03-07 | 2025-07-08 | 厦门嘉氢科技有限公司 | 用于硫酸乙烯酯合成的催化剂和清洁合成工艺 |
| CN115872974B (zh) * | 2022-12-01 | 2024-09-13 | 无锡零一未来新材料技术研究院有限公司 | 一种环状硫酸酯的后处理方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5023342A (en) * | 1988-05-26 | 1991-06-11 | Massachusetts Institute Of Technology | Cyclic sulfate compounds |
| FR2647449B1 (fr) * | 1989-05-23 | 1994-03-25 | Rhone Poulenc Sante | Procede de preparation d'ethers aromatiques |
-
1988
- 1988-03-08 FR FR8802917A patent/FR2628423B1/fr not_active Expired - Lifetime
-
1989
- 1989-03-06 AU AU31016/89A patent/AU617768B2/en not_active Ceased
- 1989-03-06 AT AT89400619T patent/ATE81339T1/de not_active IP Right Cessation
- 1989-03-06 ES ES89400619T patent/ES2045481T3/es not_active Expired - Lifetime
- 1989-03-06 IE IE890717A patent/IE890717L/xx unknown
- 1989-03-06 DE DE8989400619T patent/DE68903120T2/de not_active Expired - Fee Related
- 1989-03-06 EP EP89400619A patent/EP0332521B1/fr not_active Expired - Lifetime
- 1989-03-06 ZA ZA891693A patent/ZA891693B/xx unknown
- 1989-03-06 CA CA000592820A patent/CA1322375C/fr not_active Expired - Fee Related
- 1989-03-07 DK DK110289A patent/DK110289A/da not_active Application Discontinuation
- 1989-03-07 IL IL8951889A patent/IL89518A/en unknown
- 1989-03-07 JP JP1053061A patent/JPH0285276A/ja active Pending
- 1989-03-07 NO NO890970A patent/NO171678C/no unknown
- 1989-03-07 YU YU47589A patent/YU46890B/sh unknown
- 1989-03-07 AR AR89313357A patent/AR244678A1/es active
- 1989-03-07 MX MX015167A patent/MX169507B/es unknown
- 1989-03-07 SU SU894613609A patent/SU1720488A3/ru active
- 1989-03-07 HU HU891114A patent/HU201750B/hu not_active IP Right Cessation
- 1989-03-07 KR KR1019890002803A patent/KR910003712B1/ko not_active Expired
- 1989-03-07 FI FI891074A patent/FI92484C/fi not_active IP Right Cessation
- 1989-03-08 PT PT89946A patent/PT89946B/pt not_active IP Right Cessation
- 1989-03-08 CN CN89102590A patent/CN1025498C/zh not_active Expired - Fee Related
- 1989-09-06 US US07/403,444 patent/US4960904A/en not_active Expired - Fee Related
-
1990
- 1990-04-12 US US07/507,799 patent/US5116999A/en not_active Expired - Fee Related
-
1992
- 1992-10-08 GR GR920400441T patent/GR3005893T3/el unknown
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