SU688120A3 - Способ получени циклопропанкарбонильного соединени - Google Patents
Способ получени циклопропанкарбонильного соединениInfo
- Publication number
- SU688120A3 SU688120A3 SU782577947A SU2577947A SU688120A3 SU 688120 A3 SU688120 A3 SU 688120A3 SU 782577947 A SU782577947 A SU 782577947A SU 2577947 A SU2577947 A SU 2577947A SU 688120 A3 SU688120 A3 SU 688120A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- cis
- acid
- dibromoethyl
- formula
- cyclopropanecarbonyl
- Prior art date
Links
- -1 cyclopropanecarbonyl compound Chemical class 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 3
- 239000002253 acid Substances 0.000 claims description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Chemical group 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 230000031709 bromination Effects 0.000 claims 1
- 238000005893 bromination reaction Methods 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 238000002474 experimental method Methods 0.000 claims 1
- 238000001640 fractional crystallisation Methods 0.000 claims 1
- 150000008282 halocarbons Chemical class 0.000 claims 1
- 229910052736 halogen Chemical group 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- CHLAOFANYRDCPD-UJURSFKZSA-N (1s,3r)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carbonyl chloride Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@@H]1C(Cl)=O CHLAOFANYRDCPD-UJURSFKZSA-N 0.000 description 1
- DJSKFSCGZFZIFL-UHFFFAOYSA-N 1,1-dibromo-2-chloroethene Chemical compound ClC=C(Br)Br DJSKFSCGZFZIFL-UHFFFAOYSA-N 0.000 description 1
- BFNMOMYTTGHNGJ-UHFFFAOYSA-N 2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)CC1C(O)=O BFNMOMYTTGHNGJ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C61/16—Unsaturated compounds
- C07C61/40—Unsaturated compounds containing halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH169277A CH625777A5 (en) | 1977-02-11 | 1977-02-11 | Process for the preparation of cyclopropanecarboxylic acids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU688120A3 true SU688120A3 (ru) | 1979-09-25 |
Family
ID=4216372
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU782577947A SU688120A3 (ru) | 1977-02-11 | 1978-02-09 | Способ получени циклопропанкарбонильного соединени |
Country Status (4)
| Country | Link |
|---|---|
| AT (1) | AT354414B (de) |
| BE (1) | BE863840A (de) |
| CH (1) | CH625777A5 (de) |
| SU (1) | SU688120A3 (de) |
-
1977
- 1977-02-11 CH CH169277A patent/CH625777A5/de not_active IP Right Cessation
-
1978
- 1978-02-09 SU SU782577947A patent/SU688120A3/ru active
- 1978-02-10 AT AT96778A patent/AT354414B/de not_active IP Right Cessation
- 1978-02-10 BE BE185057A patent/BE863840A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATA96778A (de) | 1979-06-15 |
| CH625777A5 (en) | 1981-10-15 |
| AT354414B (de) | 1979-01-10 |
| BE863840A (fr) | 1978-08-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FR2379506A1 (fr) | Nouveaux esters d'acide cycloproprane carboxylique d'alcools benzyliques halogenes, leur procede de preparation et leur application comme insecticides et acaricides | |
| FR2382426A1 (fr) | Nouveaux derives phenoxybenzyloxycarbonyliques substitues, leur procede de preparation et leur application comme insecticides et acaricides | |
| DE1543805B1 (de) | Substituierte 3-Furylmethylester und Verfahren zu deren Herstellung sowie deren Verwendung als Insekticide | |
| EP0031199A1 (de) | Substituierte Benzylester von Cyclopropancarbonsäuren und deren Herstellung, diese enthaltende Zusammensetzungen und Verfahren zur Bekämpfung schädlicher Insekten damit und substituierte Benzylalkohole | |
| ES8306702A1 (es) | "un procedimiento para fabricar un compuesto de 1,1'-bifenil-3-ilmetilo sustuido". | |
| DE2738150A1 (de) | 3-styryl-2,2-dimethylcyclopropan-1carbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide | |
| BE883909A (fr) | Procede de preparation de chloro-2proprionate d'alcoyle par chloration de lactate d'alcoyle | |
| JPS61293949A (ja) | a−イソプロピル−p−クロルフエニル酢酸の光学分割法 | |
| SU688120A3 (ru) | Способ получени циклопропанкарбонильного соединени | |
| DE3788861T2 (de) | Fluorbenzylester. | |
| US3666798A (en) | Production of optically active chrysanthemic acid | |
| HU186407B (en) | Process for the production of cyclopropane-carboxylic acid ester derivatives | |
| GB1596903A (en) | Insecticidal and acaricidal phenyl alkanoic acid esters | |
| US4285969A (en) | Pyrethroids | |
| Anderson et al. | Synthesis and insecticidal activity of the stereoisomers of. alpha.-cyano-3-phenoxybenzyl 2-[2-chloro-4-(trifluoromethyl) anilino]-3-methylbutanoate (fluvalinate) and related analogs | |
| ATE2513T1 (de) | (+/-)-trans-3-(e,z-2-chlor-2-(4-chlor-phenyl)vinyl)-,2,2-dimethyl-cyclopropancarbonsaeure-(+/ )-(alpha-cyano-3-phenoxy-4-fluorbenzyl)-ester, die einzelnen e- und z-isomeren, verfahren zur herstellung dieser verbindungen, ihre verwendung als ektoparasitizide und ihre zwischenprodukte. | |
| US3981919A (en) | Racemization of optically active allethrolone | |
| JPH0556330B2 (de) | ||
| FR2398041A2 (fr) | Esters d'acides cyclopropane carboxylique comportant un substituant polyhalogene, procede de preparation et leur application comme insecticides, acaricides, nematicides et comme medicaments veterinaires | |
| US3364106A (en) | 5-tert-butyl-2-chlorophenyl nmethylcarbamate and its use as an insecticide | |
| EP0311086A1 (de) | N-fluorierte Sulfonamide, Verfahren zu deren Herstellung und deren Verwendung | |
| JPS5547694A (en) | Optically active organic thiophosphoryl chloride | |
| SU857108A1 (ru) | Способ получени бензилацетата | |
| AT375242B (de) | Insektizides mittel | |
| GB2053903A (en) | Optically active substituted pyridylmethyl esters of cyclopropanecarboxylic acids |