JPS5519219A - Methylenecryptand and its preparation - Google Patents

Methylenecryptand and its preparation

Info

Publication number
JPS5519219A
JPS5519219A JP9132878A JP9132878A JPS5519219A JP S5519219 A JPS5519219 A JP S5519219A JP 9132878 A JP9132878 A JP 9132878A JP 9132878 A JP9132878 A JP 9132878A JP S5519219 A JPS5519219 A JP S5519219A
Authority
JP
Japan
Prior art keywords
formula
cryptand
diamide
methylenecryptand
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
JP9132878A
Other languages
Japanese (ja)
Inventor
Hiroshi Kakiuchi
Masao Tomoi
Osamu Abe
Kazuaki Kihara
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 Chemical Corp
Original Assignee
Mitsubishi Chemical Industries 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 Mitsubishi Chemical Industries Ltd filed Critical Mitsubishi Chemical Industries Ltd
Priority to JP9132878A priority Critical patent/JPS5519219A/en
Publication of JPS5519219A publication Critical patent/JPS5519219A/en
Pending legal-status Critical Current

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  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

NEW MATERIAL:Methylenecryptand[2,2,1]diamide of formula I and methylene- cryptand[2,2,2]diamide of formula II.
USE: The starting material for producing fixed cryptand that is useful as interphase shifting catalyst and agent for capturing heavy metals. The resulting fixed cryptand is readily recovered and low toxicity.
PREPARATION: Methyleneazacrown ether of formula III is reacted with di- or triglycoloyl chloride of formula IV (n is 1,2) to form the objective compound of formula I or II. The reaction is effected in an inert solvent of benzene in the presence of a base as triethylamine for neutralizing the evolving hydrogen chloride at room temperature.
COPYRIGHT: (C)1980,JPO&Japio
JP9132878A 1978-07-26 1978-07-26 Methylenecryptand and its preparation Pending JPS5519219A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9132878A JPS5519219A (en) 1978-07-26 1978-07-26 Methylenecryptand and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9132878A JPS5519219A (en) 1978-07-26 1978-07-26 Methylenecryptand and its preparation

Publications (1)

Publication Number Publication Date
JPS5519219A true JPS5519219A (en) 1980-02-09

Family

ID=14023374

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9132878A Pending JPS5519219A (en) 1978-07-26 1978-07-26 Methylenecryptand and its preparation

Country Status (1)

Country Link
JP (1) JPS5519219A (en)

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