GB772979A - Preparation of pure adiponitrile - Google Patents

Preparation of pure adiponitrile

Info

Publication number
GB772979A
GB772979A GB23277/55A GB2327755A GB772979A GB 772979 A GB772979 A GB 772979A GB 23277/55 A GB23277/55 A GB 23277/55A GB 2327755 A GB2327755 A GB 2327755A GB 772979 A GB772979 A GB 772979A
Authority
GB
United Kingdom
Prior art keywords
adiponitrile
hydroxylamine
treatment
preparation
sulphuric
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
GB23277/55A
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 GB772979A publication Critical patent/GB772979A/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

Adiponitrile contaminated with by-products is purified by heating it with a hydroxylamine salt of hydrochloric, nitric, sulphuric or phosphoric acid, or a hydroxylamine acid salt of sulphuric or phosphoric acid, and thereafter separating the adiponitrile from the reaction mixture. The impure adiponitrile may be subjected to an initial hydrolysis to convert imino groups in impurities to keto groups and the resulting aqueous solution may be used directly for the hydroxylamine treatment. The treatment temperature is preferably between 100 DEG and 250 DEG C. and the purified adiponitrile may be isolated from the treatment mixture by distillation or selective solvation. The examples describe the preparation of pure adiponitrile from the crude mixture obtained by catalytic hydrogenation of dicyanobutene. Specification 667,207 is referred to.
GB23277/55A 1954-09-13 1955-08-12 Preparation of pure adiponitrile Expired GB772979A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US772979XA 1954-09-13 1954-09-13

Publications (1)

Publication Number Publication Date
GB772979A true GB772979A (en) 1957-04-17

Family

ID=22137258

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23277/55A Expired GB772979A (en) 1954-09-13 1955-08-12 Preparation of pure adiponitrile

Country Status (1)

Country Link
GB (1) GB772979A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109071421A (en) * 2016-05-02 2018-12-21 英威达纺织(英国)有限公司 The method for reducing the CPI in dintrile stream

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109071421A (en) * 2016-05-02 2018-12-21 英威达纺织(英国)有限公司 The method for reducing the CPI in dintrile stream
US11028045B2 (en) 2016-05-02 2021-06-08 Inv Nylon Chemicals Americas, Llc Process for reducing CPI in a dinitrile stream

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