JPS5711968A - Preparation of 2,2,4-trimethyl-1,2-dihydroquinoline - Google Patents

Preparation of 2,2,4-trimethyl-1,2-dihydroquinoline

Info

Publication number
JPS5711968A
JPS5711968A JP8735380A JP8735380A JPS5711968A JP S5711968 A JPS5711968 A JP S5711968A JP 8735380 A JP8735380 A JP 8735380A JP 8735380 A JP8735380 A JP 8735380A JP S5711968 A JPS5711968 A JP S5711968A
Authority
JP
Japan
Prior art keywords
catalyst
titled substance
reaction
substance
substances
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
JP8735380A
Other languages
Japanese (ja)
Inventor
Takashi Kojima
Etsuo Yamaka
Hideo Nagasaki
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP8735380A priority Critical patent/JPS5711968A/en
Publication of JPS5711968A publication Critical patent/JPS5711968A/en
Pending legal-status Critical Current

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  • Quinoline Compounds (AREA)

Abstract

PURPOSE: To obtain the titled substance in high yield, by condensing aniline with an acetone in the presence of an acidic catalyst, distilling away the titled substance and substances having lower boiling points than the titled substance, and reusing the resultant distillation residue as the acidic catalyst for the reaction described above.
CONSTITUTION: Aniline is condensed with an acetone in the presence of a nonvolatile acidic catalyst, e.g. a sulfonic acid, and the titled substance and substances, e.g. the unreacted aniline, having lower boiling points than the titled substance are distilled away. The resultant residue containing the active catalyst is directly used as the acidic catalyst in the next condensing reaction. The distillation residue is a brown to dark brown tarry substance obtained after distilling most of the substances described above from the reaction product at a temperature in the range of 100W 300°C, and usable as the catalyst 4W5 times. However, the activity is lost gradually, and a small amount of the catalyst is preferably added to keep the reaction rate.
EFFECT: Reduced residues formed as a by-product and simplified steps for removing the catalyst.
COPYRIGHT: (C)1982,JPO&Japio
JP8735380A 1980-06-26 1980-06-26 Preparation of 2,2,4-trimethyl-1,2-dihydroquinoline Pending JPS5711968A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8735380A JPS5711968A (en) 1980-06-26 1980-06-26 Preparation of 2,2,4-trimethyl-1,2-dihydroquinoline

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8735380A JPS5711968A (en) 1980-06-26 1980-06-26 Preparation of 2,2,4-trimethyl-1,2-dihydroquinoline

Publications (1)

Publication Number Publication Date
JPS5711968A true JPS5711968A (en) 1982-01-21

Family

ID=13912506

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8735380A Pending JPS5711968A (en) 1980-06-26 1980-06-26 Preparation of 2,2,4-trimethyl-1,2-dihydroquinoline

Country Status (1)

Country Link
JP (1) JPS5711968A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55126383U (en) * 1979-02-26 1980-09-06
JPS6197479U (en) * 1984-12-04 1986-06-23

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55126383U (en) * 1979-02-26 1980-09-06
JPS6197479U (en) * 1984-12-04 1986-06-23

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