GB722475A - Compositions for combatting pests containing acetylene carbinols as active ingredients thereof - Google Patents

Compositions for combatting pests containing acetylene carbinols as active ingredients thereof

Info

Publication number
GB722475A
GB722475A GB22785/52A GB2278552A GB722475A GB 722475 A GB722475 A GB 722475A GB 22785/52 A GB22785/52 A GB 22785/52A GB 2278552 A GB2278552 A GB 2278552A GB 722475 A GB722475 A GB 722475A
Authority
GB
United Kingdom
Prior art keywords
acetylene
compounds
chlorophenyl
bis
bromophenyl
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
Application number
GB22785/52A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
National Starch and Chemical Investment Holding Corp
Original Assignee
JR Geigy AG
National Starch and Chemical Investment Holding Corp
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.)
Filing date
Publication date
Application filed by JR Geigy AG, National Starch and Chemical Investment Holding Corp filed Critical JR Geigy AG
Publication of GB722475A publication Critical patent/GB722475A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/04Acyclic alcohols with carbon-to-carbon triple bonds
    • C07C33/042Acyclic alcohols with carbon-to-carbon triple bonds with only one triple bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Halogenated acetylene carbinols of the general formula <FORM:0722475/IV (b)/1> (wherein the X's represent fluorine, chlorine or bromine and may be the same or different) are prepared by reacting a ketone of the general formula <FORM:0722475/IV (b)/2> (wherein the X's are as above defined) with a metal acetylide or with acetylene in the presence of alkali hydroxide or alkali amide. In an example, potassium hydroxide in cooled dry tetrahydrofuran is saturated with acetylene, ethereal 4 : 41-difluorobenzophenone added dropwise, acetylene again passed in, and after standing 1 : 1-bis-(41-fluorophenyl) propine-2-ol-1 is isolated by treatment with ice, ether extraction and fractionation. The corresponding 1 : 1 - bis - (41-chlorophenyl)-; 1 : 1 - bis - 41 - bromophenyl)-; 1 - (41 - chlorophenyl) - 1 - (411 - bromophenyl)-; 1 - (41 - fluorophenyl) - 1 - (411-chlorophenyl)- and 1-(41-fluorophenyl)-1-(411 - bromophenyl) - propine - 2 - ol - 1 compounds are similarly prepared. The products are useful as pesticides (see Group VI)ALSO:Pesticidal compositions comprise an acetylene carbinol of the general formula <FORM:0722475/VI/1> (wherein the X's represent fluorine, chlorine or bromine and may be the same or different) together with a solid pulverulent carrier, a wetting agent or protective colloid or emulsifying agent or an inert organic liquid having an initial b.pt. above 105 DEG C. The composition may be emulsified or dispersed in aqueous medium and may incorporate other fungicidal, bactericidal, acaricidal, ovicidal or insecticidal agents e.g. benzyl benzoate; 2.7-dimethyl thianthrene; phthalonitrile; a : a -bis (p-chlorophenyl) b :b :b -trichlorethane, or -b :b -dichlorethane; 1 : 2 : 4 : 5 : 6 : 8 : 8-octachloro -3a : 4 : 7 : 7a -tetrahydro -4 : 7 -methanoindane; diethyl - p - nitrophenyl - thiophosphate; 5 : 5 -dimethyl dihydro resorcinol -N : N- di-methyl carbamate; 4 : 6 -dinitro-o-cresol; nitrated naphthylamines; mercury compounds; copper compounds and sulphur. Specified pulverulent carriers are talc, kaolin, bentonite, chalk, silicic acid, tricalcium phosphate, whiting, limestone, bole, magnesia usta, kieselguhr, boric acid, powdered cork, and powdered wood. Specified inert solvents are castor oil, paraffin oil, hydrogenated naphthalenes, alkylated naphthalenes, solvent naphtha, kerosene, and xylene. Specified emulsifying and dispersing agents are natural and synthetic soaps, turkey red oil, fatty alcohol sulphonates, sulphonated fats and fatty acid esters, high molecular quarternary ammonium compounds, ethylene oxide condensation products with aliphatic or araliphatic compounds (e.g. stearyl alcohol, alkyl phenols), sodium dibutyl naphthalene sulponate, and sulphite waste liquor. The compositions may be applied by dusting, spraying and other known methods.
GB22785/52A 1951-09-13 1952-09-11 Compositions for combatting pests containing acetylene carbinols as active ingredients thereof Expired GB722475A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH722475X 1951-09-13

Publications (1)

Publication Number Publication Date
GB722475A true GB722475A (en) 1955-01-26

Family

ID=4531653

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22785/52A Expired GB722475A (en) 1951-09-13 1952-09-11 Compositions for combatting pests containing acetylene carbinols as active ingredients thereof

Country Status (3)

Country Link
CH (1) CH300839A (en)
FR (1) FR1068853A (en)
GB (1) GB722475A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1028561B (en) * 1955-03-12 1958-04-24 Asta Werke Ag Chem Fab Process for the production of anticholinergic salts of basic ethers of diphenyl-ethynyl-carbinols
DE2756031A1 (en) * 1977-12-15 1979-06-28 Bayer Ag 1-HALOGEN-1-PROPIN-3-OLE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS FUNGICIDES
DE3122263A1 (en) * 1981-06-04 1982-12-23 Bayer Ag, 5090 Leverkusen FUNGICIDES FOR MATERIAL PROTECTION

Also Published As

Publication number Publication date
FR1068853A (en) 1954-07-01
CH300839A (en) 1954-08-31

Similar Documents

Publication Publication Date Title
GB1570982A (en) Substituted benzyl ethers and thioethers
GB722475A (en) Compositions for combatting pests containing acetylene carbinols as active ingredients thereof
US2583425A (en) Fungicidal compositions containing chlorinated isophorone
US2553772A (en) Parasiticidal compositions of olefins and perchloromethyl mercaptan
US3642910A (en) 1 1-di(p-substituted phenyl)-2 2-dichlorocyclopropanes
EP0014999A1 (en) Optically active forms of 4-(3-(p-tert.-butylphenyl)-2-methylpropyl)-cis-2,6-dimethylmorpholine and their salts; fungicides containing these compounds and process for their preparation
US3007787A (en) Butyl xylyl sulfone
US3142614A (en) Polyvalent organo-lead fungicide
US2459526A (en) 1-naphthylmethyl tetradecyl ether as an insecticide
CH632241A5 (en) Benzyl oxime ethers with pesticidal activity
US2979522A (en) Dialkyl nitroalkyl dithiophosphates
US2613226A (en) Benzyl-tert.-octylamine
US2904421A (en) Method of destroying grasses
US3412132A (en) 2-branched alkyl-4, 6-dinitrophenyl alkyl carbonates
US2545176A (en) Fungicidal compositions comprising n, n&#39;-bis (4-nitrosophenyl) piperazine
US3010871A (en) Method of destroying mites employing the p-bromophenyl ester of benzenesulfonic acid
US2451085A (en) Insecticidal haloido-alkylene esters of caprylphenoxyacetic acid
US2303683A (en) Insecticidal composition
US2653864A (en) Method of destroying plants
US2988472A (en) Method for control of soil borne pathogenic organisms
GB705037A (en) Improvements in and relating to insecticides and acaricides
US2726980A (en) Insect repellant amines produced by reacting 1, 3-butadiene and ammonia and method of using same
US2488497A (en) 1, 4-di(aryloxy)-2-butenes
US3454662A (en) 3,3-dichloropropyne
US3463822A (en) Substituted aromatic vinyl oxy thioethers