JPS5519221A - Production of fixed crown - Google Patents

Production of fixed crown

Info

Publication number
JPS5519221A
JPS5519221A JP9133078A JP9133078A JPS5519221A JP S5519221 A JPS5519221 A JP S5519221A JP 9133078 A JP9133078 A JP 9133078A JP 9133078 A JP9133078 A JP 9133078A JP S5519221 A JPS5519221 A JP S5519221A
Authority
JP
Japan
Prior art keywords
formula
crosslinked polystyrene
chloromethylated
hydroxythiacrown
effected
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
JP9133078A
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 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
Priority to JP9133078A priority Critical patent/JPS5519221A/en
Publication of JPS5519221A publication Critical patent/JPS5519221A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:The reaction of a chloromethylated and crosslinked polystyrene with hydroxythiacrown is effected to produce title substance that is useful as interphase shifting catalyst or agent for capturing heavy metals, readily recovered and low toxicity. CONSTITUTION:A chloromethylated and crosslinked polystyrene is reacted with hydroxythiacrown of formula I to form said fixed crown containing the structure of formula II (P means the crosslinked polystyrene) as a part. The reaction is effected in an inert solvent as THF in the presence of a base at 0-100 deg.C. It is desirable that at first the hydroxy-thiacrown is reacted with a base as sodium hydride, then with the chloromethylated and crosslinked polystyrene. The compound of formula I is used in an excessive amount, preferably 1-10 moles of the compound of formula I per 1 gram equivalent of chlorine atom.
JP9133078A 1978-07-26 1978-07-26 Production of fixed crown Pending JPS5519221A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9133078A JPS5519221A (en) 1978-07-26 1978-07-26 Production of fixed crown

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9133078A JPS5519221A (en) 1978-07-26 1978-07-26 Production of fixed crown

Publications (1)

Publication Number Publication Date
JPS5519221A true JPS5519221A (en) 1980-02-09

Family

ID=14023430

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9133078A Pending JPS5519221A (en) 1978-07-26 1978-07-26 Production of fixed crown

Country Status (1)

Country Link
JP (1) JPS5519221A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999062898A3 (en) * 1998-06-02 2000-02-17 Betzdearborn Inc Thiacrown ether compound
WO2000052004A1 (en) * 1999-03-01 2000-09-08 The Regents Of The University Of California Thiacrown polymers for removal of mercury from waste streams
US6187227B1 (en) 1998-06-02 2001-02-13 Betzdearborn Thiacrown ether compound corrosion inhibitors for alkanolamine units

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999062898A3 (en) * 1998-06-02 2000-02-17 Betzdearborn Inc Thiacrown ether compound
US6187227B1 (en) 1998-06-02 2001-02-13 Betzdearborn Thiacrown ether compound corrosion inhibitors for alkanolamine units
WO2000052004A1 (en) * 1999-03-01 2000-09-08 The Regents Of The University Of California Thiacrown polymers for removal of mercury from waste streams

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