GB1031907A - Method of manufacturing caprolactam - Google Patents

Method of manufacturing caprolactam

Info

Publication number
GB1031907A
GB1031907A GB2613563A GB2613563A GB1031907A GB 1031907 A GB1031907 A GB 1031907A GB 2613563 A GB2613563 A GB 2613563A GB 2613563 A GB2613563 A GB 2613563A GB 1031907 A GB1031907 A GB 1031907A
Authority
GB
United Kingdom
Prior art keywords
nitrosyl
acid
caprolactam
chloroanhydrosulphate
manufacturing
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
GB2613563A
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.)
Mitsubishi Kasei Corp
Original Assignee
Mitsubishi Kasei Corp
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 Mitsubishi Kasei Corp filed Critical Mitsubishi Kasei Corp
Publication of GB1031907A publication Critical patent/GB1031907A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D201/00Preparation, separation, purification or stabilisation of unsubstituted lactams
    • C07D201/02Preparation of lactams
    • C07D201/10Preparation of lactams from cycloaliphatic compounds by simultaneous nitrosylation and rearrangement

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Caprolactam is prepared by reacting hexahydrobenzoic acid with nitrosyl-chloroanhydrosulphate at a temperature of - 20 DEG to 200 DEG C. The molar ratio of nitrosyl-chloroanhydro-sulphate to hexahydrobenzoic acid may be 1: 0.5-8, preferably 1: 0.6-1.5. The reaction may be carried out in the presence of a small quantity, usually 0.05 to 5.0 mols. per mole of nitrosyl-chloroanhydrosulphate, of an inorganic acid or anhydride thereof or a sulphonic acid.
GB2613563A 1962-07-02 1963-07-02 Method of manufacturing caprolactam Expired GB1031907A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2747362 1962-07-02

Publications (1)

Publication Number Publication Date
GB1031907A true GB1031907A (en) 1966-06-02

Family

ID=12222068

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2613563A Expired GB1031907A (en) 1962-07-02 1963-07-02 Method of manufacturing caprolactam

Country Status (1)

Country Link
GB (1) GB1031907A (en)

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