GB897275A - Production of acrylonitrile cyclic dimer - Google Patents

Production of acrylonitrile cyclic dimer

Info

Publication number
GB897275A
GB897275A GB41938/60A GB4193860A GB897275A GB 897275 A GB897275 A GB 897275A GB 41938/60 A GB41938/60 A GB 41938/60A GB 4193860 A GB4193860 A GB 4193860A GB 897275 A GB897275 A GB 897275A
Authority
GB
United Kingdom
Prior art keywords
water
acrylonitrile
less
pressure
prepared
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
GB41938/60A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and 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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB897275A publication Critical patent/GB897275A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles

Landscapes

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

Abstract

Acrylonitrile cyclic dimers are prepared by heating acrylonitrile in the vapour phase at a pressure of at least 1000 p.s.i. out of contact with stainless steel, copper, or any other non-noble metal and/or in the presence of water at a pH of less than 8. The process may be carried out in a platinum-, glass- or silver-lined pressure-resistant vessel, in the presence or absence of water at a pH of less than 8; or in any suitable vessel in the presence of water at a pH of less than 8. The acidity may be provided by the presence of water-soluble amine acceptors, such as CO2, sulphuric, phosphoric and sulphurous acids, potassium hydrogen phosphates, oxalic, hydroxyacetic, trimethylacetic, propionic, butyric, succinic, acrylic and acetic acids, and water-soluble phenols. The preferred quantity of water is 0.3%-10% based on the acrylonitrile charged. Adiponitrile may be prepared by hydrogenation of acrylonitrile cyclic dimers at atmospheric pressure at 175 DEG C.-400 DEG C. in the presence of a reduced cobalt oxide catalyst.
GB41938/60A 1959-12-07 1960-12-06 Production of acrylonitrile cyclic dimer Expired GB897275A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US897275XA 1959-12-07 1959-12-07

Publications (1)

Publication Number Publication Date
GB897275A true GB897275A (en) 1962-05-23

Family

ID=22219301

Family Applications (1)

Application Number Title Priority Date Filing Date
GB41938/60A Expired GB897275A (en) 1959-12-07 1960-12-06 Production of acrylonitrile cyclic dimer

Country Status (1)

Country Link
GB (1) GB897275A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3202697A (en) * 1963-06-21 1965-08-24 Standard Oil Co Process for making cyclobutane-1, 2-dicyanide from acrylonitrile
US3316288A (en) * 1963-06-06 1967-04-25 Knapsack Ag Process for the manufacture of 1, 2-dicyanocyclobutane

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3316288A (en) * 1963-06-06 1967-04-25 Knapsack Ag Process for the manufacture of 1, 2-dicyanocyclobutane
US3202697A (en) * 1963-06-21 1965-08-24 Standard Oil Co Process for making cyclobutane-1, 2-dicyanide from acrylonitrile

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