NL8006593A - Cyclopropaanderivaten, werkwijzen ter bereiding ervan en hun toepassing. - Google Patents

Cyclopropaanderivaten, werkwijzen ter bereiding ervan en hun toepassing. Download PDF

Info

Publication number: NL8006593A
Authority: NL; Netherlands
Prior art keywords: formula; compound; preparation; methods; preparing
Prior art date: 1979-12-21

Application number

NL8006593A

Other languages

English (en)

Dutch (nl)

Original Assignee

Ciba Geigy

Priority date (The priority date 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 date listed.)

1979-12-21

Filing date

1980-12-03

Publication date

1981-07-16

1980-12-03 Application filed by Ciba Geigy filed Critical Ciba Geigy

1981-07-16 Publication of NL8006593A publication Critical patent/NL8006593A/nl

Links

238000000034 method Methods 0.000 title claims description 8
LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical class C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 22
238000002360 preparation method Methods 0.000 claims description 10
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
229910052794 bromium Chemical group 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
125000003158 alcohol group Chemical group 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
-1 dicyanotrimethylsiloxy Chemical group 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
239000000243 solution Substances 0.000 description 5
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000000203 mixture Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-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
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
238000004821 distillation Methods 0.000 description 2
230000000855 fungicidal effect Effects 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000002904 solvent Substances 0.000 description 2
FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
IFEMCSICGXTDGN-UHFFFAOYSA-N 1-[cyano-(3-phenoxyphenyl)methyl]-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Cl)Cl)C1(C(O)=O)C(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 IFEMCSICGXTDGN-UHFFFAOYSA-N 0.000 description 1
HTBZPEDBMOXWID-UHFFFAOYSA-N 3-(4-fluorophenoxy)benzaldehyde Chemical compound C1=CC(F)=CC=C1OC1=CC=CC(C=O)=C1 HTBZPEDBMOXWID-UHFFFAOYSA-N 0.000 description 1
MRLGCTNJRREZHZ-UHFFFAOYSA-N 3-phenoxybenzaldehyde Chemical compound O=CC1=CC=CC(OC=2C=CC=CC=2)=C1 MRLGCTNJRREZHZ-UHFFFAOYSA-N 0.000 description 1
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000012267 brine Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 1
150000001942 cyclopropanes Chemical class 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
239000003480 eluent Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
235000015497 potassium bicarbonate Nutrition 0.000 description 1
239000011736 potassium bicarbonate Substances 0.000 description 1
229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
235000011181 potassium carbonates Nutrition 0.000 description 1
TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
LEIMLDGFXIOXMT-UHFFFAOYSA-N trimethylsilyl cyanide Chemical compound C[Si](C)(C)C#N LEIMLDGFXIOXMT-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)

NL8006593A 1979-12-21 1980-12-03 Cyclopropaanderivaten, werkwijzen ter bereiding ervan en hun toepassing. NL8006593A (nl)

Applications Claiming Priority (6)

Application Number	Priority Date	Filing Date	Title
CH1140779		1979-12-21
CH1140779		1979-12-21
CH475180		1980-06-20
CH475180		1980-06-20
CH799580		1980-10-27
CH799580		1980-10-27

Publications (1)

Publication Number	Publication Date
NL8006593A true NL8006593A (nl)	1981-07-16

Family

ID=27174975

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8006593A NL8006593A (nl)	1979-12-21	1980-12-03	Cyclopropaanderivaten, werkwijzen ter bereiding ervan en hun toepassing.

Country Status (6)

Country	Link
US (1)	US4309555A (fr)
DE (1)	DE3047833A1 (fr)
FR (1)	FR2473045A1 (fr)
GB (1)	GB2067211A (fr)
IT (1)	IT8026822A0 (fr)
NL (1)	NL8006593A (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3140632A1 (de)	1981-10-13	1983-04-21	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von (alpha)-dicyano-trimethylsilyloxy-verbindungen (i)
DE3310954A1 (de) *	1983-03-25	1984-10-11	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von substituierten trialkylsilyloxymalonsaeuredinitrilen

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2657226A (en) *	1952-11-22	1953-10-27	Gen Electric	Novel cyanoalkoxy silanes
US2776306A (en) *	1953-12-31	1957-01-01	Gen Electric	Cyanoisopropylsilanes
US2985679A (en) *	1959-08-03	1961-05-23	Union Carbide Corp	Chlorocyanoalkyl silanes and siloxanes
GB1002460A (en) *	1963-08-09	1965-08-25	Midland Silicones Ltd	Organosilicon polymers
GB1227428A (fr) *	1968-04-08	1971-04-07
DE2506798A1 (de) *	1975-02-18	1976-08-26	Basf Ag	Verfahren zur herstellung von alpha-trialkylsiloxi-acrylnitrilen
DE2506805A1 (de) *	1975-02-18	1976-08-26	Basf Ag	Alpha-trialkylsiloxi-acrylnitrile
DE2721185A1 (de) *	1977-05-11	1978-11-16	Bayer Ag	Verfahren zur herstellung von substituierten vinylcyclopropancarbonsaeurebenzylestern

1980
- 1980-12-03 NL NL8006593A patent/NL8006593A/nl not_active Application Discontinuation
- 1980-12-09 US US06/214,814 patent/US4309555A/en not_active Expired - Lifetime
- 1980-12-12 GB GB8039831A patent/GB2067211A/en not_active Withdrawn
- 1980-12-18 DE DE19803047833 patent/DE3047833A1/de not_active Withdrawn
- 1980-12-19 FR FR8027148A patent/FR2473045A1/fr not_active Withdrawn
- 1980-12-19 IT IT8026822A patent/IT8026822A0/it unknown

Also Published As

Publication number	Publication date
DE3047833A1 (de)	1981-09-17
IT8026822A0 (it)	1980-12-19
US4309555A (en)	1982-01-05
FR2473045A1 (fr)	1981-07-10
GB2067211A (en)	1981-07-22

Legal Events

Date	Code	Title	Description
1983-08-01	BV	The patent application has lapsed

Publication	Publication Date	Title
JPH0127053B2 (fr)	1989-05-26
US4263319A (en)	1981-04-21	4-Substituted-2-indanol insecticidal ester derivatives
DK158784B (da)	1990-07-16	Cyklopropanderivater og insekticide midler indeholdende disse samt fremgangsmaade til bekaempelse af insekt- eller mideskadedyr under anvendelse af derivaterne eller midlerne
BRPI0507475B1 (pt)	2014-08-12	2-haloge-nofuril/tienil-3-carboxamidas, seu uso, seu processo de produção, seus intermediários, agente e seu processo de produção, e processo para controle de microorganismos indesejáveis
JPH0557269B2 (fr)	1993-08-23
IE44988B1 (en)	1982-06-02	Novel substituted phenoxybenzyloxy carbonyl derivatives, and their use as insecticides and acaricides
NL8006593A (nl)	1981-07-16	Cyclopropaanderivaten, werkwijzen ter bereiding ervan en hun toepassing.
DE69714145T2 (de)	2002-12-12	1,4-Diaryl-2-fluoro-2-butene als insectizide und akarizide Mittel
AU611014B2 (en)	1991-05-30	A pyrazole compound and its production and use
CA1237439A (fr)	1988-05-31	Derives d'acide 2,2-dimethylcyclopropane-carboxylique
DE4206917A1 (de)	1993-09-09	Verfahren zur herstellung von 1-fluorcyclopropyl-methyl-keton
JPS6136823B2 (fr)	1986-08-20
CA1248130A (fr)	1989-01-03	Pyretroides
GB1587352A (en)	1981-04-01	Cyclopropanecarboxylic acid esters
US4335252A (en)	1982-06-15	Insecticidal pyrethroid enantiomer pair
CS214680B2 (en)	1982-05-28	Method of making the optically active derivatives of cyclopropancyrboxyle acid
US4599358A (en)	1986-07-08	Pyrethroids
EP0008333A1 (fr)	1980-03-05	Alcools alpha-prop-1-inyl-phénoxybenzyliques, leur préparation et leur utilisation comme produits intermédiaires pour la préparation de pesticides
DK159771B (da)	1990-12-03	Fremgangsmaade til fremstillingen af cyklopropancarboxylsyreestere
CA1141389A (fr)	1983-02-15	Emploi comme insecticides d'esters d'acide cyclopropane-carboxylique a substitution par un groupement fluoroalcenyle
AU602980B2 (en)	1990-11-01	Novel carboxylic acid esters, method for their production and insecticides containing them as an active ingredient
AU745695B2 (en)	2002-03-28	1,4-diaryl-2,3-difluoro-2-butene insecticidal and acaricidal agents
JPS63132860A (ja)	1988-06-04	シクロプロパン化合物、その製造法及びそれを含有する殺虫組成物
CS208457B2 (en)	1981-09-15	Insicticide and acaricide means and method of making the active substances
JPH0136470B2 (fr)	1989-07-31