GB722475A - Compositions for combatting pests containing acetylene carbinols as active ingredients thereof - Google Patents
Compositions for combatting pests containing acetylene carbinols as active ingredients thereofInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C33/04—Acyclic alcohols with carbon-to-carbon triple bonds
- C07C33/042—Acyclic 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.
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)
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 |
-
1951
- 1951-09-13 CH CH300839D patent/CH300839A/en unknown
-
1952
- 1952-09-11 GB GB22785/52A patent/GB722475A/en not_active Expired
- 1952-09-12 FR FR1068853D patent/FR1068853A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1068853A (en) | 1954-07-01 |
CH300839A (en) | 1954-08-31 |
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