GB1040122A - Process for preparing monochloro-ªŠ-caprolactams - Google Patents

Process for preparing monochloro-ªŠ-caprolactams

Info

Publication number
GB1040122A
GB1040122A GB1299664A GB1299664A GB1040122A GB 1040122 A GB1040122 A GB 1040122A GB 1299664 A GB1299664 A GB 1299664A GB 1299664 A GB1299664 A GB 1299664A GB 1040122 A GB1040122 A GB 1040122A
Authority
GB
United Kingdom
Prior art keywords
caprolactams
hcl
monochloro
nocl
mixture
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
GB1299664A
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.)
Toray Industries Inc
Original Assignee
Toyo Rayon Co 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 Toyo Rayon Co Ltd filed Critical Toyo Rayon Co Ltd
Publication of GB1040122A publication Critical patent/GB1040122A/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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)

Abstract

A mixture of monochloro-e -caprolactams, mainly b - and g -chloro, is obtained by irradiating with light a mixture of monochlorocyclohexane and a nitrosation agent at -20 DEG to 50 DEG C., and subjecting the resulting monochlorocyclohexanone oxime hydrochloride to a Beckmann rearrangement at 90-150 DEG C., directly or after neutralization to free oxime. Specified nitrosation agents are NOCl, NO + Cl2, NO + NO2 + HCl, NOCl + HCl, and NO + Cl2 + HCl. Some caprolactam is also obtained in the examples, and one example also prepares cyclohexanone oxime hydrochloride from cyclohexane.
GB1299664A 1963-04-01 1964-03-26 Process for preparing monochloro-ªŠ-caprolactams Expired GB1040122A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1676663 1963-04-01

Publications (1)

Publication Number Publication Date
GB1040122A true GB1040122A (en) 1966-08-24

Family

ID=11925328

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1299664A Expired GB1040122A (en) 1963-04-01 1964-03-26 Process for preparing monochloro-ªŠ-caprolactams

Country Status (2)

Country Link
DE (1) DE1289847B (en)
GB (1) GB1040122A (en)

Also Published As

Publication number Publication date
DE1289847B (en) 1969-02-27

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