JPS56166186A - Production of cyclic acetal - Google Patents

Production of cyclic acetal

Info

Publication number
JPS56166186A
JPS56166186A JP7048780A JP7048780A JPS56166186A JP S56166186 A JPS56166186 A JP S56166186A JP 7048780 A JP7048780 A JP 7048780A JP 7048780 A JP7048780 A JP 7048780A JP S56166186 A JPS56166186 A JP S56166186A
Authority
JP
Japan
Prior art keywords
cyclic acetal
epoxyalcohol
oxygen
reaction
membered ring
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
JP7048780A
Other languages
Japanese (ja)
Other versions
JPH0131511B2 (en
Inventor
Takao Maki
Kenji Murayama
Yoshio Asahi
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 JP7048780A priority Critical patent/JPS56166186A/en
Publication of JPS56166186A publication Critical patent/JPS56166186A/en
Publication of JPH0131511B2 publication Critical patent/JPH0131511B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE: The reaction between a 1,2-epoxyalcohol and a carbonyl compound in the presence of an acid catalyst affords the titled compound having an oxygen-containing five-membered ring used as a synthetic intermediate of insecticide in high selectivity.
CONSTITUTION: The reaction of a 1,2-epoxyalcohol such as glycidol, 3,4-epoxy-2- methylpentan-2-ol, 2,3-epoxycyclopentan-1-ol with a carbonyl compound such as formaldehyde, acetaldehyde or cyclohexanecarbaldehyde is conducted in the presence of an acid catalyst such as iron chloride, aluminum bromide or p-toluenesulfonic acid to produce a cyclic acetal bearing an oxygen-containing five-membered ring such as 2-hydroxy-8,8-dimethyl-7,9-dioxabicyclo[4,3,0]nonane.
COPYRIGHT: (C)1981,JPO&Japio
JP7048780A 1980-05-27 1980-05-27 Production of cyclic acetal Granted JPS56166186A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7048780A JPS56166186A (en) 1980-05-27 1980-05-27 Production of cyclic acetal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7048780A JPS56166186A (en) 1980-05-27 1980-05-27 Production of cyclic acetal

Publications (2)

Publication Number Publication Date
JPS56166186A true JPS56166186A (en) 1981-12-21
JPH0131511B2 JPH0131511B2 (en) 1989-06-26

Family

ID=13432919

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7048780A Granted JPS56166186A (en) 1980-05-27 1980-05-27 Production of cyclic acetal

Country Status (1)

Country Link
JP (1) JPS56166186A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8969598B2 (en) 2011-06-24 2015-03-03 Eastman Chemical Company Production of cyclic acetals or ketals using liquid-phase acid catalysts
US9000229B2 (en) 2011-06-24 2015-04-07 Eastman Chemical Company Production of hydroxy ether hydrocarbons by vapor phase hydrogenolysis of cyclic acetals and ketals
US9056313B2 (en) 2011-06-24 2015-06-16 Eastman Chemical Company Catalysts for the production of hydroxy ether hydrocarbons by vapor phase hydrogenolysis of cyclic acetals and ketals
US9315485B2 (en) 2011-06-24 2016-04-19 Eastman Chemical Company Production of cyclic acetals by reactive distillation
US9382179B2 (en) 2011-06-24 2016-07-05 Eastman Chemical Company Nickel modified catalyst for the production of hydroxy ether hydrocarbons by vapor phase hydrogenolysis of cyclic acetals and ketals
US9388105B2 (en) 2011-06-24 2016-07-12 Eastman Chemical Company Production of hydroxy ether hydrocarbons by liquid phase hydrogenolysis of cyclic acetals or cyclic ketals
US9440944B2 (en) 2011-06-24 2016-09-13 Eastman Chemical Company Production of cyclic acetals or ketals using solid acid catalysts

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
TETRA HEDRON *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8969598B2 (en) 2011-06-24 2015-03-03 Eastman Chemical Company Production of cyclic acetals or ketals using liquid-phase acid catalysts
US9000229B2 (en) 2011-06-24 2015-04-07 Eastman Chemical Company Production of hydroxy ether hydrocarbons by vapor phase hydrogenolysis of cyclic acetals and ketals
US9056313B2 (en) 2011-06-24 2015-06-16 Eastman Chemical Company Catalysts for the production of hydroxy ether hydrocarbons by vapor phase hydrogenolysis of cyclic acetals and ketals
US9315485B2 (en) 2011-06-24 2016-04-19 Eastman Chemical Company Production of cyclic acetals by reactive distillation
US9382179B2 (en) 2011-06-24 2016-07-05 Eastman Chemical Company Nickel modified catalyst for the production of hydroxy ether hydrocarbons by vapor phase hydrogenolysis of cyclic acetals and ketals
US9388105B2 (en) 2011-06-24 2016-07-12 Eastman Chemical Company Production of hydroxy ether hydrocarbons by liquid phase hydrogenolysis of cyclic acetals or cyclic ketals
US9394271B2 (en) 2011-06-24 2016-07-19 Eastman Chemical Company Production of cyclic acetals or ketals using liquid-phase acid catalysts
US9440944B2 (en) 2011-06-24 2016-09-13 Eastman Chemical Company Production of cyclic acetals or ketals using solid acid catalysts

Also Published As

Publication number Publication date
JPH0131511B2 (en) 1989-06-26

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