GB969091A - Mixed sulphite diesters - Google Patents

Mixed sulphite diesters

Info

Publication number
GB969091A
GB969091A GB2302762A GB2302762A GB969091A GB 969091 A GB969091 A GB 969091A GB 2302762 A GB2302762 A GB 2302762A GB 2302762 A GB2302762 A GB 2302762A GB 969091 A GB969091 A GB 969091A
Authority
GB
United Kingdom
Prior art keywords
sulphite
tert
propargyl
isopropyl
butynyl
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
GB2302762A
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.)
Uniroyal Inc
Original Assignee
United States Rubber Co
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 United States Rubber Co filed Critical United States Rubber Co
Publication of GB969091A publication Critical patent/GB969091A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C301/00Esters of sulfurous acid
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N41/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/02Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C301/00Esters of sulfurous acid
    • C07C301/02Esters of sulfurous acid having sulfite groups bound to carbon atoms of six-membered aromatic rings

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)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises mixed sulphite esters of the formula: <FORM:0969091/C1/1> where R is an aliphatic or cycloaliphatic radical, e.g. alkyl, cycloalkyl, alkenyl, cyanoalkyl or haloalkyl or an aromatic radical, unsubstituted or substituted by, for example, one or more of alkyl, cycloalkyl, haloalkyl, alkoxy, nitro and halo; R1 is an acyclic alkynyl radical; n is 2-10 and m is 1-10. Where m is greater than 1 the repeating alkoxy groups may be the same or different. The esters are prepared from the chlorosulphinates of the glycol ethers by treatment in a solvent, for example, benzene, xylene or solvent naphtha with the alkynyl alcohol in the presence of an HCl acceptor, for example, pyridine, dimethyl-aniline or trimethylamine at between -10 DEG and 50 DEG C. The compounds may be used as insecticides (see Division A5). Chlorosulphinates of the formula <FORM:0969091/C1/2> wherein n, m and R have the above significance are prepared by treatment of the required glycol ethers with thionyl chloride at between -5 DEG and 30 DEG C. Glycol ethers of the formula <FORM:0969091/C1/3> wherein n, m and R have the above significance, are prepared by reacting the required alcohols and phenols with alkylene oxides.ALSO:Insecticidal compositions contain sulphite esters of the formula <FORM:0969091/A5-A6/1> where R is an aliphatic or cycloaliphatic radical, e.g. alkyl, cycloalkyl, alkenyl, cyanoalkyl or haloalkyl or an aromatic radical which may be unsubstituted or substituted by, for example, one or more of alkyl, cycloalkyl, haloalkyl, alkoxy, nitro and halo; R1 is an acyclic alkynyl radical; n is 2-10 and m is 1-10 (see Division C2). The chemicals may be applied as dusts mixed with powdered solid carriers; for example talc, mica, pyrophyllite and clays; as liquids or sprays when dissolved in a solvent, for example acetone, benzene or kerosene or as aerosol sprays when dissolved directly in an aerosol carrier. They are preferably used in aqueous emulsions containing an anionic, non-ionic or cationic surface-active dispersing agent or aqueous suspensions containing solid wettable powder carriers containing surface-active dispersing agents. Examples describe the use of propargyl p-tert. butylphenoxy isopropyl sulphite, propergyl p-tert. butyl phenoxy isopropoxy isopropyl sulphite and propargyl p-tert. butyl phenoxy diisopropoxy isopropyl sulphite in the control of mosquito larv and propargyl p-tert. butyl phenoxy isopropyl sulphite, propargyl p-tert. butyl phenoxy isopropoxy isopropyl sulphite, propargyl p-tert. butyl phenoxy diisopropoxy isopropyl sulphite, propargyl p-tert. amylphenoxymethyl sulphite, propargyl isodecoxyethyl sulphite, propargyl o-tert. butylphenoxy isopropoxy isopropyl sulphite, 1-(3-butynyl) p-tert. amylphenoxy ethyl sulphite, 2-(3-butynyl) p-tert. amylphenoxyethyl sulphite, 2 - (2 - methyl - 3 - butynyl) - p - tert. amylphenoxyethyl sulphite, 2-(3-hexynyl) p-tert. amylphenoxyethyl sulphite, 2-(3-butynyl) o-tert. butylphenoxy isopropoxy isopropyl sulphite and 1-(2-butynyl) p-tert. amylphenoxyethyl sulphite in the control of mites. The compositions may contain other insecticides, fungicides and bactericides.
GB2302762A 1961-08-16 1962-06-15 Mixed sulphite diesters Expired GB969091A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US13174161A 1961-08-16 1961-08-16

Publications (1)

Publication Number Publication Date
GB969091A true GB969091A (en) 1964-09-09

Family

ID=22450817

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2302762A Expired GB969091A (en) 1961-08-16 1962-06-15 Mixed sulphite diesters

Country Status (6)

Country Link
BE (1) BE619254A (en)
CH (1) CH408907A (en)
DE (1) DE1567199A1 (en)
GB (1) GB969091A (en)
LU (1) LU41941A1 (en)
NL (1) NL121168C (en)

Also Published As

Publication number Publication date
DE1567199A1 (en) 1970-01-29
LU41941A1 (en) 1962-08-25
NL121168C (en) 1966-09-15
CH408907A (en) 1966-03-15
BE619254A (en) 1962-10-15
NL280837A (en) 1964-12-10

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