CN103936723A - 一种催化三唑烯环氧化制备氟环唑的方法 - Google Patents
一种催化三唑烯环氧化制备氟环唑的方法 Download PDFInfo
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- CN103936723A CN103936723A CN201310024555.5A CN201310024555A CN103936723A CN 103936723 A CN103936723 A CN 103936723A CN 201310024555 A CN201310024555 A CN 201310024555A CN 103936723 A CN103936723 A CN 103936723A
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- epoxiconazole
- triazole
- catalysis
- preparing
- triazole alkene
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
- B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
- B01J31/1815—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
- B01J31/2217—At least one oxygen and one nitrogen atom present as complexing atoms in an at least bidentate or bridging ligand
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
- B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
- B01J31/223—At least two oxygen atoms present in one at least bidentate or bridging ligand
- B01J31/2234—Beta-dicarbonyl ligands, e.g. acetylacetonates
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/70—Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
- B01J2231/72—Epoxidation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
- B01J2531/0238—Complexes comprising multidentate ligands, i.e. more than 2 ionic or coordinative bonds from the central metal to the ligand, the latter having at least two donor atoms, e.g. N, O, S, P
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/70—Complexes comprising metals of Group VII (VIIB) as the central metal
- B01J2531/72—Manganese
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Epoxy Compounds (AREA)
Abstract
Description
Claims (10)
Priority Applications (1)
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CN201310024555.5A CN103936723B (zh) | 2013-01-23 | 2013-01-23 | 一种催化三唑烯环氧化制备氟环唑的方法 |
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CN201310024555.5A CN103936723B (zh) | 2013-01-23 | 2013-01-23 | 一种催化三唑烯环氧化制备氟环唑的方法 |
Publications (2)
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CN103936723A true CN103936723A (zh) | 2014-07-23 |
CN103936723B CN103936723B (zh) | 2016-06-29 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108371957A (zh) * | 2018-03-27 | 2018-08-07 | 吕桂兰 | 一种纳米功能材料选择性环氧化制备化妆品香料中间体的方法 |
CN111848504A (zh) * | 2019-04-29 | 2020-10-30 | 沈阳中化农药化工研发有限公司 | 一种锰催化剂及其催化三唑烯环氧化制备氟环唑的应用 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0427061A2 (de) * | 1989-11-04 | 1991-05-15 | BASF Aktiengesellschaft | Verfahren zur Herstellung von cis-2-(1H-1,2,4-Triazol-1-yl-methyl)-2-halogenphenyl)-3-(Halogenphenyl)-oxiran |
WO2004000835A1 (de) * | 2002-06-24 | 2003-12-31 | Basf Aktiengesellschaft | Verfahren zur herstellung von 1,2,4-triazolylmethyl-oxiranen |
CN1995049A (zh) * | 2006-12-29 | 2007-07-11 | 湖南师范大学 | 8-羟基喹啉衍生物的锰催化剂及其在烯烃环氧化中的应用 |
CN101513183A (zh) * | 2008-02-18 | 2009-08-26 | 北京绿色农华植保科技有限责任公司 | 一种稳定的氟环唑原药制备方法 |
-
2013
- 2013-01-23 CN CN201310024555.5A patent/CN103936723B/zh active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0427061A2 (de) * | 1989-11-04 | 1991-05-15 | BASF Aktiengesellschaft | Verfahren zur Herstellung von cis-2-(1H-1,2,4-Triazol-1-yl-methyl)-2-halogenphenyl)-3-(Halogenphenyl)-oxiran |
WO2004000835A1 (de) * | 2002-06-24 | 2003-12-31 | Basf Aktiengesellschaft | Verfahren zur herstellung von 1,2,4-triazolylmethyl-oxiranen |
CN1995049A (zh) * | 2006-12-29 | 2007-07-11 | 湖南师范大学 | 8-羟基喹啉衍生物的锰催化剂及其在烯烃环氧化中的应用 |
CN101513183A (zh) * | 2008-02-18 | 2009-08-26 | 北京绿色农华植保科技有限责任公司 | 一种稳定的氟环唑原药制备方法 |
Non-Patent Citations (3)
Title |
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PATTAMA SAISAHA,等: "Manganese catalyzed cis-dihydroxylation of electron deficient alkenes with H2O2", 《ORG. BIOMOL. CHEM.》, vol. 8, 31 December 2010 (2010-12-31), pages 4444 - 4450 * |
江才鑫,等: "氟环唑的合成综述", 《浙江化工》, vol. 37, no. 10, 31 October 2006 (2006-10-31), pages 9 - 10 * |
闫立单,等: "氟环唑的合成新工艺", 《中国农药》, no. 12, 31 December 2012 (2012-12-31), pages 14 - 16 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108371957A (zh) * | 2018-03-27 | 2018-08-07 | 吕桂兰 | 一种纳米功能材料选择性环氧化制备化妆品香料中间体的方法 |
CN108371957B (zh) * | 2018-03-27 | 2021-03-16 | 深圳伊赞泉化妆品有限公司 | 一种纳米功能材料选择性环氧化制备化妆品香料中间体的方法 |
CN111848504A (zh) * | 2019-04-29 | 2020-10-30 | 沈阳中化农药化工研发有限公司 | 一种锰催化剂及其催化三唑烯环氧化制备氟环唑的应用 |
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Effective date of registration: 20160114 Address after: 110021 Liaodong Road, Tiexi District, Liaoning, No. 8-1, No. Applicant after: SHENYANG SINOCHEM PESTICIDE CHEMICAL RESEARCH AND DEVELOPMENT CO., LTD. Address before: 100031 Beijing, Xicheng District, the door of the revitalization of the main street, No. 28 Applicant before: Sinochem Corporation Applicant before: Shenyang Research Institute of Chemical Industry |
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