GB775085A - Preparations for combating pests - Google Patents

Preparations for combating pests

Info

Publication number
GB775085A
GB775085A GB23481/52A GB2348152A GB775085A GB 775085 A GB775085 A GB 775085A GB 23481/52 A GB23481/52 A GB 23481/52A GB 2348152 A GB2348152 A GB 2348152A GB 775085 A GB775085 A GB 775085A
Authority
GB
United Kingdom
Prior art keywords
same meaning
specified
general formula
compound
halogen
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
GB23481/52A
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.)
BASF Schweiz AG
Original Assignee
Ciba AG
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 Ciba AG filed Critical Ciba AG
Publication of GB775085A publication Critical patent/GB775085A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/38Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
    • C07F9/40Esters thereof
    • C07F9/4003Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/4006Esters of acyclic acids which can have further substituents on alkyl

Abstract

A compound of the general formula <FORM:0775085/IV(b)/1> (in which R1 and R2 each represent an alkyl, cycloalkyl, aralkyl, aryl or heterocyclic residue, and may be members of a ring system, and may contain substituents; R4 represents hydrogen, halogen, or has the same meaning as R1; R5 represents hydrogen or the residue -OR1, SR1, -NH2, -NHR1 or -NR1R2, or has the same meaning as R1; X and Y each represent -O-, -S-, -NH-, or -N-R1-; Z represents oxygen or sulphur; and Hal represents halogen) may be prepared by reacting a compound of the general formula <FORM:0775085/IV(b)/2> (in which R3 has the same meaning as R1) with a compound of the general formula <FORM:0775085/IV(b)/3> in molecular proportions. The reactants may be diluted with an inert solvent, e.g. benzene, toluene, ether, dioxane, hexane or benzine. Cooling may be necessary. The reaction may be brought to an end by heating to 50-120 DEG C. The reaction product may be distilled off under reduced pressure. The radicals R1, R2 and R3 may be methyl, ethyl, propyl, isopropyl, butyl, hexyl, 2-ethylbutyl, octyl, 2-butyloctyl, lauryl, octadecyl, allyl, and 2-chloroethyl and may contain thiocyanic acid, cyano or ester groups; phenyl, 2- and 4-chlorophenyl, 2 : 4-dichlorophenyl, 4-methoxyphenyl, 4-nitrophenyl, naphthyl and 4-diphenyl; benzyl; cyclohexyl; or tetrahydrofurfuryl. The phosphorus-containing reactant may be trimethyl, triethyl, tripropyl, diethyl - lauryl, tri - (2 - chlorethyl), ethyl ethylene glycol, 2 : 4-dichlorophenyl-diethyl, or 4-chlorophenyl-dimethyl phosphite. The other reactant may be dichloracetaldehyde, beutyl-chloral, bromal or chloral; 1 : 1-dichloracetone, 1 : 1 : 3 - trichloracetone, 1 : 1 : 1 - trichloracetone, 1 : 1 : 3 : 3 - tetrachloracetone, 1 : 1 : 3 : 3 - tetrachloracetone, penta- or hexa-chloracetone, o - trichloracetophenone, 4 - chloro - o - trichloracetophenone or 4-methyl-o - trichloracetophenone; trichloracetic acid ethyl ester; and trichloracetic acid dimethylamide. Specifications 723,633, 744,360 and 747,824 are referred to.ALSO:A pesticide comprises a compound of the general formula:-<FORM:0775085/VI/1> (in which R1 and R2 each represent an alkyl, cycloakyl, aralkyl, aryl or heterocyclic residue, and may be members of a ring system and may contain substituents; R4 represents hydrogen, halogen, or has the same meaning as R1; R5 represents hydorgen or the residue - OR1, - SR1, - NH2, -NHR1 or -NR1R2, or has the same meaning as R1; X and Y each represents - O -, -S-, - NH-, or - N - R1-; Z represents oxygen or sulphur; and Hal represents halogen), in admixture with a solid diluent, or with a liquid diluent and an emulsifying agent. For compounds specified (see Group IV(b). Solid diluents specified are kaolin, gypsum and bentonite. Liquid diluents specified are alcohol, petroleum, tar distillates, n-buotanol spindle oil, diethylene glycol. The condensation product of tertiary dodecyl mercaptan and ethylene oxide is specified as emulsifying agents. Other ingredients specified are oleic acid, sulphite cellulose waste liquor and cellulose derivatives. Specifications 723,633, 744,360 and 747,824 [all in Group IV(b)] are referred to.
GB23481/52A 1951-09-25 1952-09-18 Preparations for combating pests Expired GB775085A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH775085X 1951-09-25

Publications (1)

Publication Number Publication Date
GB775085A true GB775085A (en) 1957-05-22

Family

ID=4535752

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23481/52A Expired GB775085A (en) 1951-09-25 1952-09-18 Preparations for combating pests

Country Status (1)

Country Link
GB (1) GB775085A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2194370A1 (en) * 1972-08-01 1974-03-01 Inst Przemyslu Organiczego
US6576661B1 (en) 1999-11-09 2003-06-10 Bayer Aktiengesellschaft Active ingredient combination having insecticidal and acaricidal characteristics
DE102007045955A1 (en) 2007-09-26 2009-04-09 Bayer Cropscience Ag Active agent combination, useful e.g. for combating animal pests and treating seeds of transgenic plants, comprises substituted amino-furan-2-one compound and at least one compound e.g. diazinon, isoxathion, carbofuran or aldicarb
US8846567B2 (en) 2009-03-25 2014-09-30 Bayer Cropscience Ag Active compound combinations having insecticidal and acaricidal properties

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2194370A1 (en) * 1972-08-01 1974-03-01 Inst Przemyslu Organiczego
US6576661B1 (en) 1999-11-09 2003-06-10 Bayer Aktiengesellschaft Active ingredient combination having insecticidal and acaricidal characteristics
US6818670B2 (en) 1999-11-09 2004-11-16 Bayer Aktiengesellschaft Active ingredient combination having insecticidal and acaricidal characteristics
DE102007045955A1 (en) 2007-09-26 2009-04-09 Bayer Cropscience Ag Active agent combination, useful e.g. for combating animal pests and treating seeds of transgenic plants, comprises substituted amino-furan-2-one compound and at least one compound e.g. diazinon, isoxathion, carbofuran or aldicarb
US8846567B2 (en) 2009-03-25 2014-09-30 Bayer Cropscience Ag Active compound combinations having insecticidal and acaricidal properties

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