GB954440A - Trihalovinylsulphenylhalides and their preparation - Google Patents

Trihalovinylsulphenylhalides and their preparation

Info

Publication number
GB954440A
GB954440A GB3601760A GB3601760A GB954440A GB 954440 A GB954440 A GB 954440A GB 3601760 A GB3601760 A GB 3601760A GB 3601760 A GB3601760 A GB 3601760A GB 954440 A GB954440 A GB 954440A
Authority
GB
United Kingdom
Prior art keywords
give
compounds
trihalovinyl
sulphides
sulphenyl
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
GB3601760A
Inventor
Edward David Weil
Keith Jacob Smith
Emil John Geering
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.)
Hooker Chemical Corp
Original Assignee
Hooker Chemical 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 Hooker Chemical Corp filed Critical Hooker Chemical Corp
Priority to GB3601760A priority Critical patent/GB954440A/en
Publication of GB954440A publication Critical patent/GB954440A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C313/00Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C313/08Sulfenic acids; Derivatives thereof
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide

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)
  • Indole Compounds (AREA)

Abstract

The invention comprises the compounds of the formula CX2:CX.SX, where each X is chlorine or bromine; the production of such compounds wherein -SX is -SCl by chlorinating the corresponding trihalovinyl di- or polysulphide; the production of trichlorovinyl sulphenyl chloride and bromide by dehydrohalogenating the corresponding tetrachloroethyl compound, e.g. with triethylamine at room temperature; and the production of N-trichlorovinyl mercaptophthalimide and -tetrahydrophthalimide by reacting CCl2:CCl.SCl with phthalimide or tetrahydrophthalimide in the presence of an acid-binding agent. In addition sulphenyl chlorides of the invention may be converted to the corresponding sulphenyl bromides by means of hydrogen bromide. The compounds of the invention are said to react with oxygen, nitric acid or hydrogen peroxide to form the corresponding sulphinic and sulphonic derivatives, with chlorine and bromine to form pentahaloethyl sulphenyl halides, with nucleophilic anions, with nitrogen bases, with reducing agents such as HI to give the corresponding disulphide, with aromatic compounds to give trihalovinyl aryl sulphides, with olefines to give 2-haloalkyl sulphides, with acetylenes to give 2-halovinyl sulphides, with H2S to give the corresponding tri- and polysulphides, with organic phosphites to give S-trihalovinyl phosphorothiolates, and with carbanions to give trihalovinyl alkyl sulphides. The compounds of the invention can be used to control soil pathogens (see Division A5). Specifications 949,374 and 949,375 are referred to.ALSO:Pathogens in soil are controlled by applying to the soil a compound of formula CX2 : CX.SX, where each X is Cl or Br (see Division C2). Similarly used is N-trichlorovinylmercaptophthalimide. Specifications 949,374 and 949,375 are referred to.
GB3601760A 1960-10-20 1960-10-20 Trihalovinylsulphenylhalides and their preparation Expired GB954440A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3601760A GB954440A (en) 1960-10-20 1960-10-20 Trihalovinylsulphenylhalides and their preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3601760A GB954440A (en) 1960-10-20 1960-10-20 Trihalovinylsulphenylhalides and their preparation

Publications (1)

Publication Number Publication Date
GB954440A true GB954440A (en) 1964-04-08

Family

ID=10384044

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3601760A Expired GB954440A (en) 1960-10-20 1960-10-20 Trihalovinylsulphenylhalides and their preparation

Country Status (1)

Country Link
GB (1) GB954440A (en)

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