GB994616A - New aliphatic isonitriles - Google Patents

New aliphatic isonitriles

Info

Publication number
GB994616A
GB994616A GB4933463A GB4933463A GB994616A GB 994616 A GB994616 A GB 994616A GB 4933463 A GB4933463 A GB 4933463A GB 4933463 A GB4933463 A GB 4933463A GB 994616 A GB994616 A GB 994616A
Authority
GB
United Kingdom
Prior art keywords
isocyanide
general formula
compounds
dichlorobenzyl
hydrogen
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
GB4933463A
Inventor
Uwe Fetzer
Ivar Ugi
Guenter Unterstenhoefer
Wolfgang Behrenz
Paul-Ernst Frohberger
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Publication of GB994616A publication Critical patent/GB994616A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C251/00Compounds containing nitrogen atoms doubly-bound to a carbon skeleton

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention relates to araliphatic isonitriles having a total of 7-12 carbon atoms of the general formula <FORM:0994616/C2/1> wherein R1-R5, which may be the same or different, are hydrogen or halogen atoms or inorganic or organic radicals, at least one of which is other than a hydrogen atom, and A is an unsubstituted or substituted alkylene bridge, and wherein either or both of the o-positions may be joined with A to form a ring. Compounds claimed per se are p-chlorobenzyl isocyanide, 3,4 - dichlorbenzyl isocyanide, 2 - isocyanotetralin, a ,a - dimethylbenzyl isocyanide, 2,6-dichlorobenzyl isocyanide, 2,4,6 - trichlorobenzyl isocyanide, p-methoxy-benzyl isocyanide. The compounds may be prepared by splitting water from an aralkyl formamide of the general formula <FORM:0994616/C2/2> in which R1-R5 and A have the same meanings as above; or splitting off hydrogen sulphide from an aralkyl thioformamide of the general formula <FORM:0994616/C2/3> in which R1-R5 and A have the same meanings as above; or reacting an aralkyl amine of the general formula <FORM:0994616/C2/4> in which R1-R5 and A have the same meanings as above with dichlorocarbene-forming agent and an alkali metal hydroxide or alcoholate. Examples describe the preparation of each of the above specified compounds. Specified substituents R1-R5 are NO2, CN, OMe, diMe, 3,4-dimethylene, 4 -isopropyl, 2,4,6 - trimethyl, 3-chloro - 4 - methyl, 3 - nitro - 4 - methyl, and 3,4-methylene dioxide.ALSO:Pesticidal compositions comprise as active ingredient an isonitrile of the general formula <FORM:0994616/A5-A6/1> wherein R1-R5 which may be the same or different are hydrogen or halogen atoms or inorganic or organic radicals, at least one of which is other than a hydrogen atom, and A is an unsubstituted or substituted alkylene bridge, and wherein either or both of the o-positions may be joined with A to form a ring, in a mixture with a solid or liquid diluent. Specified active ingredients are 2,6 - dichlorobenzyl isocyanide, 2,3 - dichlorobenzyl isocyanide, 3,4 - dichlorobenzyl isocyanide, parachlorobenzyl isocyanide and 2,4,6 - trichlorobenzyl isocyanide. The compositions may be used in solid or liquid form alone or in admixture with solid or liquid diluents, optionally also in an emulsion, or in combination with other biocidal compounds, such as insecticides, based on phosphorus or urethane compounds.
GB4933463A 1962-12-17 1963-12-13 New aliphatic isonitriles Expired GB994616A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF38573A DE1211853B (en) 1962-12-17 1962-12-17 Insecticidal agent

Publications (1)

Publication Number Publication Date
GB994616A true GB994616A (en) 1965-06-10

Family

ID=7097398

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4933463A Expired GB994616A (en) 1962-12-17 1963-12-13 New aliphatic isonitriles

Country Status (5)

Country Link
BE (1) BE641311A (en)
DE (1) DE1211853B (en)
DK (1) DK103374C (en)
GB (1) GB994616A (en)
NL (1) NL301906A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107056635B (en) * 2017-06-09 2019-03-01 广西师范大学 A kind of synthetic method of alkynyl amide class compound

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3012932A (en) * 1959-02-19 1961-12-12 Standard Oil Co Compositions and methods employing insecticidal oil soluble organic carbylamines

Also Published As

Publication number Publication date
NL301906A (en)
BE641311A (en) 1964-04-16
DK103374C (en) 1965-12-20
DE1211853B (en) 1966-03-03

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