JPS6461435A - Production of dialkylnaphthalenes - Google Patents

Production of dialkylnaphthalenes

Info

Publication number
JPS6461435A
JPS6461435A JP21555787A JP21555787A JPS6461435A JP S6461435 A JPS6461435 A JP S6461435A JP 21555787 A JP21555787 A JP 21555787A JP 21555787 A JP21555787 A JP 21555787A JP S6461435 A JPS6461435 A JP S6461435A
Authority
JP
Japan
Prior art keywords
solvent
alcl3
catalyst
concentration
mixture
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.)
Granted
Application number
JP21555787A
Other languages
Japanese (ja)
Other versions
JPH0459301B2 (en
Inventor
Ryohei Minami
Yukio Nagao
Yasushi Idegami
Keiichi Yokota
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.)
Air Water Inc
Original Assignee
Sumikin 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 Sumikin Chemical Co Ltd filed Critical Sumikin Chemical Co Ltd
Priority to JP21555787A priority Critical patent/JPS6461435A/en
Publication of JPS6461435A publication Critical patent/JPS6461435A/en
Publication of JPH0459301B2 publication Critical patent/JPH0459301B2/ja
Granted legal-status Critical Current

Links

Landscapes

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

Abstract

PURPOSE:To increase concentration of a dialkylnaphthalene, by reacting naphthalenes with a lower olefin to provide an alkylnaphthalene mixture and isomerizing or trans-alkylating the resultant mixture in the presence of AlCl3 as a catalyst and HCl gas as a cocatalyst in a solvent. CONSTITUTION:Naphthalenes are reacted with a lower olefin (normally ethylene or propylene) in a solvent at 50-90 deg.C to provide an alkylnaphthalene mixture, which is then isomerized or trans-alkylated in a solvent (e.g. hexane or heptane) at 50-100 deg.C (preferably 50-90 deg.C) by adding AlCl3 as a catalyst and HCl gas as a cocatalyst to improve the concentration of a dialkylnaphthalene. The resultant product in the latter stage is separated into a solvent layer and a catalyst layer consisting of polyalkylnaphthalenes and the AlCl3. The obtained catalyst layer is subsequently circulated. The reaction can be carried out at the low temperature to suppress reaction forming heavy substances and the aimed substance is simultaneously obtained in a high concentration and yield.
JP21555787A 1987-08-28 1987-08-28 Production of dialkylnaphthalenes Granted JPS6461435A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21555787A JPS6461435A (en) 1987-08-28 1987-08-28 Production of dialkylnaphthalenes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21555787A JPS6461435A (en) 1987-08-28 1987-08-28 Production of dialkylnaphthalenes

Publications (2)

Publication Number Publication Date
JPS6461435A true JPS6461435A (en) 1989-03-08
JPH0459301B2 JPH0459301B2 (en) 1992-09-21

Family

ID=16674400

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21555787A Granted JPS6461435A (en) 1987-08-28 1987-08-28 Production of dialkylnaphthalenes

Country Status (1)

Country Link
JP (1) JPS6461435A (en)

Also Published As

Publication number Publication date
JPH0459301B2 (en) 1992-09-21

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