JPS5655362A - Polyfunctional azide compound and its preparation - Google Patents

Polyfunctional azide compound and its preparation

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Publication number
JPS5655362A
JPS5655362A JP12982079A JP12982079A JPS5655362A JP S5655362 A JPS5655362 A JP S5655362A JP 12982079 A JP12982079 A JP 12982079A JP 12982079 A JP12982079 A JP 12982079A JP S5655362 A JPS5655362 A JP S5655362A
Authority
JP
Japan
Prior art keywords
formula
acid
azide compound
group
preparation
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.)
Pending
Application number
JP12982079A
Other languages
Japanese (ja)
Inventor
Kazumi Okawa
Yoichi Saito
Kaoru Iwata
Akihiro Horiie
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.)
Teijin Ltd
Original Assignee
Teijin 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 Teijin Ltd filed Critical Teijin Ltd
Priority to JP12982079A priority Critical patent/JPS5655362A/en
Publication of JPS5655362A publication Critical patent/JPS5655362A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

NEW MATERIAL:A polyfunctional azide compound of formula I(R is 3W12C p-valent aliphatic group which may contain O atom; p is 3W6).
EXAMPLE: Penterythritol tetrakisazidobenzoic acid ester.
USE: A photosensitive material and a crosslinking agent. It has high crosslinking ability, and is highly soluble in various solvents. It also has high compatiblity with resist polymers such as cyclized rubber, and can be prepared economically.
PROCESS: The compound of formula I is prepared by reacting a polyol of formula II with an azidobenzoic acid of formula III [Q is OH, halogen, -OZ (Z is univalent hydrocarbon group) or group or formula IV]. The reaction is carried out in a solvent such as hexane, and if necessary, in the presence of a catalyst or an acid aceceptor.
COPYRIGHT: (C)1981,JPO&Japio
JP12982079A 1979-10-11 1979-10-11 Polyfunctional azide compound and its preparation Pending JPS5655362A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12982079A JPS5655362A (en) 1979-10-11 1979-10-11 Polyfunctional azide compound and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12982079A JPS5655362A (en) 1979-10-11 1979-10-11 Polyfunctional azide compound and its preparation

Publications (1)

Publication Number Publication Date
JPS5655362A true JPS5655362A (en) 1981-05-15

Family

ID=15019023

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12982079A Pending JPS5655362A (en) 1979-10-11 1979-10-11 Polyfunctional azide compound and its preparation

Country Status (1)

Country Link
JP (1) JPS5655362A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7897797B2 (en) * 2006-09-08 2011-03-01 The University Of Massachusetts Cyclooctene monomers
EP3941167A1 (en) * 2020-07-17 2022-01-19 Basf Se Thin metal electrode films, and manufacturing method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7897797B2 (en) * 2006-09-08 2011-03-01 The University Of Massachusetts Cyclooctene monomers
EP3941167A1 (en) * 2020-07-17 2022-01-19 Basf Se Thin metal electrode films, and manufacturing method thereof
WO2022012937A1 (en) * 2020-07-17 2022-01-20 Basf Se Thin metal electrode films, and manufacturing method thereof

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