JPS5520742A - Alpha-substituted amino-epsilon-caprolactam - Google Patents

Alpha-substituted amino-epsilon-caprolactam

Info

Publication number
JPS5520742A
JPS5520742A JP9405478A JP9405478A JPS5520742A JP S5520742 A JPS5520742 A JP S5520742A JP 9405478 A JP9405478 A JP 9405478A JP 9405478 A JP9405478 A JP 9405478A JP S5520742 A JPS5520742 A JP S5520742A
Authority
JP
Japan
Prior art keywords
caprolactam
formula
epsilon
alpha
substituted amino
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.)
Granted
Application number
JP9405478A
Other languages
Japanese (ja)
Other versions
JPS6241233B2 (en
Inventor
Haruyo Satou
Shinzo Imamura
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
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP9405478A priority Critical patent/JPS5520742A/en
Publication of JPS5520742A publication Critical patent/JPS5520742A/en
Publication of JPS6241233B2 publication Critical patent/JPS6241233B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Plural Heterocyclic Compounds (AREA)
  • Polyamides (AREA)
  • Epoxy Resins (AREA)

Abstract

NEW MATERIAL:α-Substrituted amino-ε-caprolactams of formula I (R1 is formula II; R2 is H, formula II).
EXAMPLE: α-Glycidylamino-ε-caprolactam.
USE: Agricultural chemicals, raw materials for polymers and intermediates of various kinds of compounds.
PREPARATION: For example, α-aminocyclohexanone oxime hydrochloride is subjected to Beckmann rearrangement to form α-amino-ε-caprolactam, which is made to react with epichlorohydrin to give α-(3-chloro-2-hydroxypropylamino)-ε-caprolactam of formula III. The product is dehydrochlorinated to produce the objective compound of formula I.
COPYRIGHT: (C)1980,JPO&Japio
JP9405478A 1978-08-01 1978-08-01 Alpha-substituted amino-epsilon-caprolactam Granted JPS5520742A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9405478A JPS5520742A (en) 1978-08-01 1978-08-01 Alpha-substituted amino-epsilon-caprolactam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9405478A JPS5520742A (en) 1978-08-01 1978-08-01 Alpha-substituted amino-epsilon-caprolactam

Publications (2)

Publication Number Publication Date
JPS5520742A true JPS5520742A (en) 1980-02-14
JPS6241233B2 JPS6241233B2 (en) 1987-09-02

Family

ID=14099823

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9405478A Granted JPS5520742A (en) 1978-08-01 1978-08-01 Alpha-substituted amino-epsilon-caprolactam

Country Status (1)

Country Link
JP (1) JPS5520742A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7939657B2 (en) 2003-10-29 2011-05-10 Elan Pharmaceuticals, Inc. N-substituted benzene sulfonamides

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7939657B2 (en) 2003-10-29 2011-05-10 Elan Pharmaceuticals, Inc. N-substituted benzene sulfonamides

Also Published As

Publication number Publication date
JPS6241233B2 (en) 1987-09-02

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