MD332C2 - Method of obtaining cis-2-(1H-1,2,4-triazole-1-yl-methyl)-2-(halogenphenyl)-3-(halogenphenyl)-oxirane - Google Patents
Method of obtaining cis-2-(1H-1,2,4-triazole-1-yl-methyl)-2-(halogenphenyl)-3-(halogenphenyl)-oxiraneInfo
- Publication number
- MD332C2 MD332C2 MD95-0016A MD950016A MD332C2 MD 332 C2 MD332 C2 MD 332C2 MD 950016 A MD950016 A MD 950016A MD 332 C2 MD332 C2 MD 332C2
- Authority
- MD
- Moldova
- Prior art keywords
- halogenphenyl
- triazole
- oxirane
- methyl
- restorer
- Prior art date
Links
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- C07D231/12—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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Epoxy Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention relates to the method of obtaining cis-2-(1H-1,2,4-triazole-1-yl-methyl)-2-(halogenphenyl)-3-(halogenphenyl)-oxirane with the following formula:The purpose of the invention is to increase the going out of the product with a special purpose and to diminish the cleaning expenses.The method if put into practice by the epoxidation of Z-3-(1H-1,2,4-triazole-1-yl)-2-(halogenphenyl)-1-(halogenphenyl)-propene with Permalloy acid with a further renewal. As a restorer may be used sodium hydrosulfite, sodium dithion or sodium thiosulfate or hydrogen in the presence of rhenium nickel. the restorer is added to the reaction composition in a quantity exceeding the quantity which is necessary for the dissociation of probably existing Permalloy acid.Claims:2
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3936821A DE3936821A1 (en) | 1989-11-04 | 1989-11-04 | METHOD FOR PRODUCING CIS-2- (1H-1,2,4-TRIAZOL-1-YLMETHYL) -2- (HALOGENPHENYL) -3- (HALOGENPHENYL) -OXIRAN |
SU904831490A RU2071473C1 (en) | 1989-11-04 | 1990-11-02 | Process for preparing cis-2-(1h-triazol-1-yl-methyl)-2- (halogenphenyl)-3-(halogenphenyl)oxirane |
Publications (2)
Publication Number | Publication Date |
---|---|
MD332B1 MD332B1 (en) | 1995-11-30 |
MD332C2 true MD332C2 (en) | 1996-03-31 |
Family
ID=6392916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MD95-0016A MD332C2 (en) | 1989-11-04 | 1994-12-13 | Method of obtaining cis-2-(1H-1,2,4-triazole-1-yl-methyl)-2-(halogenphenyl)-3-(halogenphenyl)-oxirane |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0427061B1 (en) |
JP (1) | JP2983054B2 (en) |
KR (1) | KR0157314B1 (en) |
AT (1) | ATE116315T1 (en) |
CA (1) | CA2028650C (en) |
DE (2) | DE3936821A1 (en) |
DK (1) | DK0427061T3 (en) |
ES (1) | ES2066089T3 (en) |
MD (1) | MD332C2 (en) |
RU (1) | RU2071473C1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ272586A (en) * | 1995-07-17 | 1996-10-28 | Apotex Inc | Process for preparing fluconazole and triazolylepoxypropane precursors |
EP1517906B1 (en) * | 2002-06-24 | 2007-03-28 | Basf Aktiengesellschaft | Method for the production of 1,2,4-triazolylmethyl-oxiranes |
EP2746275A1 (en) | 2012-12-19 | 2014-06-25 | Basf Se | New substituted triazoles and imidazoles and their use as fungicides |
CN103936723B (en) * | 2013-01-23 | 2016-06-29 | 沈阳中化农药化工研发有限公司 | A kind of method that catalysis triazole alkene epoxidation prepares epoxiconazole |
CN111848504A (en) * | 2019-04-29 | 2020-10-30 | 沈阳中化农药化工研发有限公司 | Manganese catalyst and application thereof in catalyzing epoxidation of triazolene to prepare epoxiconazole |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2952755A1 (en) * | 1979-12-29 | 1981-07-02 | Bayer Ag, 5090 Leverkusen | METHOD FOR PRODUCING OXIRANES |
CA1271764A (en) * | 1985-03-29 | 1990-07-17 | Stefan Karbach | Azolylmethyloxiranes, their preparation and their use as crop protection agents |
-
1989
- 1989-11-04 DE DE3936821A patent/DE3936821A1/en not_active Withdrawn
-
1990
- 1990-10-26 ES ES90120548T patent/ES2066089T3/en not_active Expired - Lifetime
- 1990-10-26 EP EP90120548A patent/EP0427061B1/en not_active Expired - Lifetime
- 1990-10-26 CA CA002028650A patent/CA2028650C/en not_active Expired - Lifetime
- 1990-10-26 DK DK90120548.4T patent/DK0427061T3/en active
- 1990-10-26 AT AT90120548T patent/ATE116315T1/en not_active IP Right Cessation
- 1990-10-26 DE DE59008135T patent/DE59008135D1/en not_active Expired - Lifetime
- 1990-11-02 JP JP2295569A patent/JP2983054B2/en not_active Expired - Lifetime
- 1990-11-02 RU SU904831490A patent/RU2071473C1/en active
- 1990-11-03 KR KR1019900017840A patent/KR0157314B1/en not_active IP Right Cessation
-
1994
- 1994-12-13 MD MD95-0016A patent/MD332C2/en not_active IP Right Cessation
Non-Patent Citations (1)
Title |
---|
Cererea nr. 3218129, DE, Int. Cl. C 07 D 405 /06, 1983. * |
Also Published As
Publication number | Publication date |
---|---|
RU2071473C1 (en) | 1997-01-10 |
ATE116315T1 (en) | 1995-01-15 |
KR910009695A (en) | 1991-06-28 |
ES2066089T3 (en) | 1995-03-01 |
EP0427061B1 (en) | 1994-12-28 |
JPH03153682A (en) | 1991-07-01 |
EP0427061A3 (en) | 1992-01-02 |
DK0427061T3 (en) | 1995-02-27 |
DE59008135D1 (en) | 1995-02-09 |
JP2983054B2 (en) | 1999-11-29 |
KR0157314B1 (en) | 1998-11-16 |
EP0427061A2 (en) | 1991-05-15 |
MD332B1 (en) | 1995-11-30 |
CA2028650A1 (en) | 1991-05-05 |
DE3936821A1 (en) | 1991-05-08 |
CA2028650C (en) | 2003-09-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG4A | Patent for invention issued | ||
IF99 | Valid patent on 19990615 |
Free format text: EXPIRES: 20101102 |
|
KA4A | Patent for invention lapsed due to non-payment of fees (with right of restoration) | ||
MM4A | Patent for invention definitely lapsed due to non-payment of fees |