JPS5636459A - Separation of isoquinoline - Google Patents

Separation of isoquinoline

Info

Publication number
JPS5636459A
JPS5636459A JP11166679A JP11166679A JPS5636459A JP S5636459 A JPS5636459 A JP S5636459A JP 11166679 A JP11166679 A JP 11166679A JP 11166679 A JP11166679 A JP 11166679A JP S5636459 A JPS5636459 A JP S5636459A
Authority
JP
Japan
Prior art keywords
isoquinoline
quarternary
quinoline base
base mixture
coal tar
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
JP11166679A
Other languages
Japanese (ja)
Inventor
Hiroshi Okazaki
Masaharu Inoue
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.)
Nippon Steel Chemical and Materials Co Ltd
Original Assignee
Nippon Steel Chemical 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 Nippon Steel Chemical Co Ltd filed Critical Nippon Steel Chemical Co Ltd
Priority to JP11166679A priority Critical patent/JPS5636459A/en
Publication of JPS5636459A publication Critical patent/JPS5636459A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: A kind of alkyl halide is used to form selectively the quarternary salt of isoquinoline from isoquinoline in a quinoline base mixture and the product is used as an anticorrosive agent directly or is decomposed to give isoquinoline.
CONSTITUTION: A quinoline base mixture such as a fraction boiling at 240W250°C which has been separated from coal tar is combined with an alkyl halide of the formula: RX (R is 1W20C substituted or unsubstituted alkyl; X is Cl, Br or I) such as lauryl chloride in an amount of 0.8W1.5 times the molar quantity of the isoquinoline in the base mixture and the reaction is effected at 100W250, preferably 100W200°C to form a quarternary alkylated compound of isoquinoline. The reaction mixture is cooled and stood to conduct the layer separation for isolation of the quarternary salt. When the fraction boiling at 240W250°C from coal tar is employed, the unreacted quinoline base is almost composed of methylquinoline, which is used as a raw material for quinophthalone pigments.
COPYRIGHT: (C)1981,JPO&Japio
JP11166679A 1979-09-03 1979-09-03 Separation of isoquinoline Pending JPS5636459A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11166679A JPS5636459A (en) 1979-09-03 1979-09-03 Separation of isoquinoline

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11166679A JPS5636459A (en) 1979-09-03 1979-09-03 Separation of isoquinoline

Publications (1)

Publication Number Publication Date
JPS5636459A true JPS5636459A (en) 1981-04-09

Family

ID=14567096

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11166679A Pending JPS5636459A (en) 1979-09-03 1979-09-03 Separation of isoquinoline

Country Status (1)

Country Link
JP (1) JPS5636459A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61237193A (en) * 1985-04-13 1986-10-22 シャープ株式会社 Window acounting machine
CN107382850A (en) * 2017-09-25 2017-11-24 贾海亮 A kind of 2 methylquinoline and its isomer and the separation method of isoquinolin

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61237193A (en) * 1985-04-13 1986-10-22 シャープ株式会社 Window acounting machine
CN107382850A (en) * 2017-09-25 2017-11-24 贾海亮 A kind of 2 methylquinoline and its isomer and the separation method of isoquinolin

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