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GB618432A - Improvements in or relating to method of forming halogenated organic compounds and the products resulting therefrom - Google Patents

Improvements in or relating to method of forming halogenated organic compounds and the products resulting therefrom

Info

Publication number
GB618432A
GB618432A GB8475/46A GB847546A GB618432A GB 618432 A GB618432 A GB 618432A GB 8475/46 A GB8475/46 A GB 8475/46A GB 847546 A GB847546 A GB 847546A GB 618432 A GB618432 A GB 618432A
Authority
GB
United Kingdom
Prior art keywords
adduct
give
carbon tetrachloride
product
dihydride
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
GB8475/46A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Publication of GB618432A publication Critical patent/GB618432A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C23/00Compounds containing at least one halogen atom bound to a ring other than a six-membered aromatic ring
    • C07C23/18Polycyclic halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C23/00Compounds containing at least one halogen atom bound to a ring other than a six-membered aromatic ring
    • C07C23/18Polycyclic halogenated hydrocarbons
    • C07C23/20Polycyclic halogenated hydrocarbons with condensed rings none of which is aromatic
    • C07C23/38Polycyclic halogenated hydrocarbons with condensed rings none of which is aromatic with three condensed rings

Landscapes

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

Abstract

Halogenated Diels-Alder adducts of a hexahalocyclopentadiene with a conjugated diene are prepared by halogenating the hexahalocyclopentadiene adduct, to give addition halogenation or substitution of halogen for hydrogen or for another halogen atom. The products are useful as insecticides. In examples: (1) chlorine is passed into a solution of the adduct of hexachlorocyclopentadiene and cyclopentadiene in carbon tetrachloride, giving octachlorodicyclopentadiene-dihydride; the same product may also be obtained by chlorination under pressure; (2) the adduct starting material of (1) is brominated in carbon tetrachloride in the absence of light and oxygen, in the presence of diphenylamine to give the expected dibromo compound; the addition of a small quantity of aluminium bromide to the reaction mixture causes the bromine to substitute to give hexachloromonobromodicyclopentadiene; (3) the starting material of (1) is treated with liquid anhydrous hydrogen fluoride and lead peroxide in chloroform solution in a steel bomb to produce the difluoride; (4) the Diels-Alder adduct of hexabromocyclopentadiene and cyclopentadiene is chlorinated in carbon tetrachloride to give the dichloro-addition product; (5) a solution of the starting material of (1) in carbon tetrachloride is treated with bromine in the presence of lauryl peroxide giving 1-bromohexachlorodicyclopentadiene; (6) the starting material of (1) is chlorinated with sulphuryl chloride in carbon tetrachloride in the presence of benzoyl peroxide to give a chloro-derivative C10H5Cl7; (7) the product of (5) is treated with sodium iodide in acetone, replacing the bromine atom with an iodine atom; (8) the product of (5) is treated with silver chloride gel, replacing the bromine atom with a chlorine atom; (9) chlorine is passed into a solution of the product of (5) in carbon tetrachloride to give a mixture of 1-chloro- and 1-bromo-octachlorodicyclopentadiene-dihydride; (10) the product of (5) is treated with chlorine and antimony pentachloride in carbon tetrachloride giving the 1-bromo-2,3-dichloro-hexachlorodicyclopentadienedihydride; (11) the adduct of hexachlorocyclopentadiene and methylcyclopentadiene is chlorinated to give a mixture of chloromethyland methyl - octachlorodicyclopentadiene - di - hydride, and (12) the adduct of hexachlorocyclopentadiene and isoprene (1,4,5,6,7,7-hexachloro-3-isopropenyl D 5-bicycloheptene-(1,2,2)) is chlorinated to give the dichloro-addition product. Specification 614,931 is referred to. p ALSO:Insecticides contain as the active ingredient a halogenated Diels-Alder adduct of a hexahalocyclopentadiene with a conjugated diolefine. The insecticides may be used as dusts, oil sprays, aerosols and water emulsions. In examples insecticides are prepared comprising a hydrocarbon oil base containing 1 per cent of an organic thiocyanate and, as the lethal constituent, (1) octacheorodicyclopentadiene dihydride; (2) and (5) a monobromo derivative of the hexachlorocyclopentadiene-cyclopentadiene adduct; (9) a mixture of 1-chloro-and 1-bromo octachlorocyclopentadiene dihydride; (11) a mixture of chloromethyl and methyl-octachlorodicyclopentadiene dihydride, and (12) the dichloride of the adduct of hexachloro-cyclopentadiene and isoprene. Specification 614,931 is referred to.
GB8475/46A 1945-07-25 1946-03-19 Improvements in or relating to method of forming halogenated organic compounds and the products resulting therefrom Expired GB618432A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US618432XA 1945-07-25 1945-07-25
US260146XA 1946-01-26 1946-01-26

Publications (1)

Publication Number Publication Date
GB618432A true GB618432A (en) 1949-02-22

Family

ID=26700604

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8475/46A Expired GB618432A (en) 1945-07-25 1946-03-19 Improvements in or relating to method of forming halogenated organic compounds and the products resulting therefrom

Country Status (2)

Country Link
GB (1) GB618432A (en)
MY (1) MY5300132A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2576666A (en) * 1949-12-07 1951-11-27 Julius Hyman & Company Process for producing heptachlor
US2598561A (en) * 1949-10-03 1952-05-27 Velsicol Corp Method for production of chlordane
US2676132A (en) * 1950-04-18 1954-04-20 Shell Dev 1,2,3,4,10,10-hexachloro-6,7-epoxy-1,4,4alpha,5,6,7,8,8alpha-octhydro-1,4,5,8-dimethanonaphthalene and insecticidal compositions thereof
DE932671C (en) * 1952-03-28 1955-09-05 Arvey Corp Process for the preparation of 1, 2, 4, 5, 6, 7, 8, 8-octachlor-3a, 4, 7, 7a-tetrahydro-4, 7-endomethyleneindane (chlordane)
US2771479A (en) * 1949-10-17 1956-11-20 Universal Oil Prod Co Insecticidal compounds
US2818445A (en) * 1949-12-03 1957-12-31 Shell Dev Process for chlorinating 4, 5, 6, 7, 8, 8-hexachloro-3a, 4, 7, 7a-tetrahydro-4, 7-methanoindene to form the corresponding 1, 2-octachloro-methanoindane
DE1035651B (en) * 1953-01-29 1958-08-07 Bataafsche Petroleum Process for the production of polycyclic pest control agents with two linearly linked bicyclo- (2, 2, 1) -heptane rings
US3154579A (en) * 1961-04-24 1964-10-27 Velsicol Chemical Corp Bis (polyhalotetrahydro-4, 7-methanoinden-1-yl)-amines
DE977345C (en) * 1952-03-23 1966-01-13 Velsicol Chemical Corp Process for the preparation of 1, 4, 5, 6, 7, 8, 8-heptachlor-3a, 4, 7, 7 a-tetrahydro-4, 7-endomethylene indene

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2598561A (en) * 1949-10-03 1952-05-27 Velsicol Corp Method for production of chlordane
US2771479A (en) * 1949-10-17 1956-11-20 Universal Oil Prod Co Insecticidal compounds
US2818445A (en) * 1949-12-03 1957-12-31 Shell Dev Process for chlorinating 4, 5, 6, 7, 8, 8-hexachloro-3a, 4, 7, 7a-tetrahydro-4, 7-methanoindene to form the corresponding 1, 2-octachloro-methanoindane
US2576666A (en) * 1949-12-07 1951-11-27 Julius Hyman & Company Process for producing heptachlor
US2676132A (en) * 1950-04-18 1954-04-20 Shell Dev 1,2,3,4,10,10-hexachloro-6,7-epoxy-1,4,4alpha,5,6,7,8,8alpha-octhydro-1,4,5,8-dimethanonaphthalene and insecticidal compositions thereof
DE977345C (en) * 1952-03-23 1966-01-13 Velsicol Chemical Corp Process for the preparation of 1, 4, 5, 6, 7, 8, 8-heptachlor-3a, 4, 7, 7 a-tetrahydro-4, 7-endomethylene indene
DE932671C (en) * 1952-03-28 1955-09-05 Arvey Corp Process for the preparation of 1, 2, 4, 5, 6, 7, 8, 8-octachlor-3a, 4, 7, 7a-tetrahydro-4, 7-endomethyleneindane (chlordane)
DE1035651B (en) * 1953-01-29 1958-08-07 Bataafsche Petroleum Process for the production of polycyclic pest control agents with two linearly linked bicyclo- (2, 2, 1) -heptane rings
US3154579A (en) * 1961-04-24 1964-10-27 Velsicol Chemical Corp Bis (polyhalotetrahydro-4, 7-methanoinden-1-yl)-amines

Also Published As

Publication number Publication date
MY5300132A (en) 1953-12-31

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