GB654980A - Improvements in and relating to the production of bodies adapted for use as insecticides - Google Patents

Improvements in and relating to the production of bodies adapted for use as insecticides

Info

Publication number
GB654980A
GB654980A GB748848A GB748848A GB654980A GB 654980 A GB654980 A GB 654980A GB 748848 A GB748848 A GB 748848A GB 748848 A GB748848 A GB 748848A GB 654980 A GB654980 A GB 654980A
Authority
GB
United Kingdom
Prior art keywords
insecticidal
hydrogen
pyridine
nickel
piperidine
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
GB748848A
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.)
DAVID WILLIAM MILNER
YORKSHIRE TAR DISTILLERS Ltd
Original Assignee
DAVID WILLIAM MILNER
YORKSHIRE TAR DISTILLERS Ltd
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 DAVID WILLIAM MILNER, YORKSHIRE TAR DISTILLERS Ltd filed Critical DAVID WILLIAM MILNER
Priority to GB748848A priority Critical patent/GB654980A/en
Publication of GB654980A publication Critical patent/GB654980A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/02Preparation by ring-closure or hydrogenation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Catalysts (AREA)

Abstract

Insecticidal compositions are produced by a process comprising catalytically hydrogenating pyridine or its homologues or catalytically dehydrogenating piperidine hydrogenated quinoline or hydrogenated isoquinoline or their homologues optionally in the presence of hydrogen and recovering an insecticidal mixture of condensation products boiling above about 275 DEG C. by fractionation. According to the Provisional Specification the mere treatment of the above classes of compounds with hydrogenation or dehydrogenation catalysts respectively enables high boiling insecticidal materials to be produced and quinoline and isoquinoline are included as starting materials and the use of hydrogen in either process appears optional. The process may be carried out in either liquid or vapour phase and the hydrogenation or dehydrogenation catalyst employed appears unimportant. Nickel, particularly Raney nickel, is a suitable catalyst showing both hydrogenation and dehydrogenation activity according to temperature. In the vapour phase operation a nickel cage may be used and Raney nickel in the liquid phase operation. Mixtures of tertiary nitrogenous cyclic bases may be used such as mixtures of pyridine and piperidine. In examples (1) pyridine vapour and hydrogen are passed over a nickel cage catalyst at elevated temperature and pressure to obtain a product containing 90 per cent piperidine and from which 5 per cent of insecticidal material is obtained by fractionation at atmospheric pressure; (2) piperidine is heated at elevated pressure in the pressure of Raney nickel with hydrogen and the products are fractionated to obtain insecticidal material boiling over 275 DEG C.ALSO:An insecticidal mixture of condensation products boiling above about 275 DEG C. is obtained by fractionation of products obtained by catalytically hydrogenating pyridine or its homologues or catalytically dehydrogenating, optionally in the presence of hydrogen, piperidine, hydrogenated quinoline or hydrogenated isoquinoline or their homologues (see Group IV(b). According to the provisional Specification the mere treatment of the above classes of compounds and quinoline and isoquinoline also with hydrogenation or dehydrogenation catalysts respectively, yields high boiling insecticidal materials, and the use of hydrogen is optional. Material boiling over 275 DEG C. having insecticidal properties is obtained by fractionating products obtained in p examples (I) by hydrogenating pyridine using a nickel catalyst; (II) by heating pyridine with hydrogen in the presence of Raney nickel.
GB748848A 1948-03-11 1948-03-11 Improvements in and relating to the production of bodies adapted for use as insecticides Expired GB654980A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB748848A GB654980A (en) 1948-03-11 1948-03-11 Improvements in and relating to the production of bodies adapted for use as insecticides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB748848A GB654980A (en) 1948-03-11 1948-03-11 Improvements in and relating to the production of bodies adapted for use as insecticides

Publications (1)

Publication Number Publication Date
GB654980A true GB654980A (en) 1951-07-04

Family

ID=9834074

Family Applications (1)

Application Number Title Priority Date Filing Date
GB748848A Expired GB654980A (en) 1948-03-11 1948-03-11 Improvements in and relating to the production of bodies adapted for use as insecticides

Country Status (1)

Country Link
GB (1) GB654980A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114797947A (en) * 2022-05-19 2022-07-29 兄弟科技股份有限公司 Efficient dehydrogenation catalyst and application thereof in preparation of pyridine by dehydrogenation of piperidine raw materials

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114797947A (en) * 2022-05-19 2022-07-29 兄弟科技股份有限公司 Efficient dehydrogenation catalyst and application thereof in preparation of pyridine by dehydrogenation of piperidine raw materials

Similar Documents

Publication Publication Date Title
Nagata et al. Biradical formation from acyclic conjugated eneyne-allene system related to neocarzinostatin and esperamicin-calichemicin
US2836628A (en) Unsaturated branched-chain alcohols and methods of preparing same
Huntsman et al. Reactions of Diolefins at High Temperatures. II. The Cyclization of 1, 6-Octadiene and 7-Methyl-1, 6-octadiene1
GB654980A (en) Improvements in and relating to the production of bodies adapted for use as insecticides
GB864926A (en) Process for preparing novel compounds of the lactone type
Koelsch et al. Hydrogenation of Hydroxyglutaconaldehyde Dianil and of 3-Hydroxy-1-phenylpyridinium Salts1
Hubert Base-catalysed prototropic isomerization. Part V. A novel method for the preparation of enamines
US3387051A (en) Method of preparation of substituted aryl ethane compounds
EMERSON The reaction of styrene with aldehydes
US3691249A (en) Dimerization of diolefinic compounds
EP0026323B1 (en) 4(5)-acetyl-9,9-dimethyltricyclo-(4,4,0,1(8,10))-undec-1-ene, its preparation and use as odorant, and odorant composition containing it
US2562487A (en) Production of 1-methylcyclopentanone-2
US2175003A (en) Process for the preparation of hexahydro-para-phenylene diamine
GB801723A (en) Purification of glycols by distillation
GB685728A (en) Improvements in the treatment of di-olefinic terpenes
DE740722C (en) Process for the preparation of basic compounds, especially the pyridine series
GB793150A (en) 1, 2, 5, 6-diepoxycyclooctane and process for the preparation thereof
DE827800C (en) Process for the production of saturated terpene aldehydes and terpene alcohols
Patterson et al. Preparation of Pyrrole
US2945067A (en) Conversion of verbanone
GB742041A (en) Improvements in or relating to the production of toluic acids
Searles Jr et al. Oxetanes. XI. The Cyclization of 3-Hydroxymethylcarvomenthol1, 2
GB641026A (en) Improvements in or relating to the preparation of reduction products of n-phenyl-3, 5-diethyl-2-propyldihydropyridine
GB756751A (en) Improvements in or relating to the production of 1-methylcyclohexene
Dewar et al. 396. Researches on phellandrenes. Part IV. A comparison of the catalytic dehydrogenation of l-α-phellandrene and l-piperitone