JPS5459209A - Preparation of methyl tert-butyl ether - Google Patents

Preparation of methyl tert-butyl ether

Info

Publication number
JPS5459209A
JPS5459209A JP12315477A JP12315477A JPS5459209A JP S5459209 A JPS5459209 A JP S5459209A JP 12315477 A JP12315477 A JP 12315477A JP 12315477 A JP12315477 A JP 12315477A JP S5459209 A JPS5459209 A JP S5459209A
Authority
JP
Japan
Prior art keywords
methanol
mixture
column
title compound
fixed bed
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
JP12315477A
Other languages
Japanese (ja)
Other versions
JPS6121212B2 (en
Inventor
Tetsuya Takesono
Yasuo Fujiwara
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.)
Eneos Corp
Original Assignee
Nippon Oil 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 Nippon Oil Corp filed Critical Nippon Oil Corp
Priority to JP12315477A priority Critical patent/JPS5459209A/en
Priority to GB48291/77A priority patent/GB1587866A/en
Priority to US05/853,192 priority patent/US4182913A/en
Priority to IT51902/77A priority patent/IT1090580B/en
Priority to FR7735029A priority patent/FR2371408A1/en
Priority to DE19772752111 priority patent/DE2752111A1/en
Publication of JPS5459209A publication Critical patent/JPS5459209A/en
Priority to US06/059,377 priority patent/US4256465A/en
Publication of JPS6121212B2 publication Critical patent/JPS6121212B2/ja
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/10—Use of additives to fuels or fires for particular purposes for improving the octane number
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/02—Use of additives to fuels or fires for particular purposes for reducing smoke development

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

PURPOSE: To obtain the title compound effectively in high yield, by reacting a isobutylene-containing dydrocarbon and methanol in a specific molar ratio, distilling reaction mexuture, and recycling an azeotrope of the title compound and methanol.
CONSTITUTION: Iosbutylene-containing hydeocarbon and methanol are reacted in a ratio of isobutylene:methanol=1:1.0-1.4 by passing the mixture through a fixed bed of particles of a strong acid type cation-exchange resin. The reaction mixture is passed through a fixed bed of a water-insoluble solid granular acid-nuetralizing agent having an average particle diameter of 0.1-10mm, and subsequently an unreacted hydrocarbon mixture is removed by distillation in a separation column. The mixture is further distilled. in a multistage distillation column, and is obtained from the top of the column. The azeotrope is recycled to the reactor and reused. The highly pure title compound is obtained from the bottom of the column. The reaction mixture after passing through the catalyst bed is devided into two parts, and the one stream is preferably recycled to the fixed bed directly.
COPYRIGHT: (C)1979,JPO&Japio
JP12315477A 1976-11-22 1977-10-14 Preparation of methyl tert-butyl ether Granted JPS5459209A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP12315477A JPS5459209A (en) 1977-10-14 1977-10-14 Preparation of methyl tert-butyl ether
GB48291/77A GB1587866A (en) 1976-11-22 1977-11-21 Methyl tert-butyl ether
US05/853,192 US4182913A (en) 1976-11-22 1977-11-21 Method for producing methyl tert-butyl ether and fuel composition containing the same
IT51902/77A IT1090580B (en) 1976-11-22 1977-11-22 METHOD TO PRODUCE METHYL-TER-BUTYL ETHER AND FUEL COMPOSITION CONTAINING THE SAME
FR7735029A FR2371408A1 (en) 1976-11-22 1977-11-22 PROCESS FOR THE PRODUCTION OF METHYL OXIDE AND TERT-BUTYL AND FUEL COMPOSITION CONTAINING THIS COMPOUND
DE19772752111 DE2752111A1 (en) 1976-11-22 1977-11-22 PROCESS FOR THE PRODUCTION OF METHYL-T-BUTYL ETHER AND A FUEL MIXTURE CONTAINING THIS ETHER
US06/059,377 US4256465A (en) 1976-11-22 1979-07-20 Method for producing methyl tert-butyl ether and fuel composition containing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12315477A JPS5459209A (en) 1977-10-14 1977-10-14 Preparation of methyl tert-butyl ether

Publications (2)

Publication Number Publication Date
JPS5459209A true JPS5459209A (en) 1979-05-12
JPS6121212B2 JPS6121212B2 (en) 1986-05-26

Family

ID=14853507

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12315477A Granted JPS5459209A (en) 1976-11-22 1977-10-14 Preparation of methyl tert-butyl ether

Country Status (1)

Country Link
JP (1) JPS5459209A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56169638A (en) * 1980-04-28 1981-12-26 Inst Francais Du Petrole Ether production by reaction of olefin with alcohol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56169638A (en) * 1980-04-28 1981-12-26 Inst Francais Du Petrole Ether production by reaction of olefin with alcohol

Also Published As

Publication number Publication date
JPS6121212B2 (en) 1986-05-26

Similar Documents

Publication Publication Date Title
US3979461A (en) Process for the preparation of methyl tert-butyl ether
US4918244A (en) Preparation of MTBE from TBA and methanol
US4250328A (en) Method for separation of an ester from a reaction mixture
FI69052C (en) FOERFARANDE FOER SAMTIDIG FRAMSTAELLNING AV REN MTB OCH I STORT SETT ISOBUTENFRI C4-KOLVAETEBLANDNING
CA1236487A (en) Process for producing acetals
US4071567A (en) Process for the production of methyl tert-butyl ether
CA1253886A (en) Process for producing methyl tertiary butyl ether
YU37302B (en) Process for the separation of isobutylene from a c4-hydrocarbon mixture
GB1564459A (en) Preparation of methacrylic derivatives
JPS59108740A (en) Esterification of acetic acid from alcohol and glycol ether having four or more carbon atomes
GB2048247B (en) Process for preparing methyl tertiary-butyl ether
CA1048062A (en) Process for the production of methyl tert-butyl ether
US4925989A (en) MTBE preparation from isobutylene/TBA and methanol in presence of an acid resin catalyst
EP0876320A1 (en) Process for the production of fluoromethylhexafluoroisopropylether
US4322565A (en) Process for purifying ethers
US4775447A (en) Process for the production of 2,2-dimethoxypropane
JPS6031522B2 (en) How to remove acidic substances from reaction products
JPH0239496B2 (en)
JPS5459209A (en) Preparation of methyl tert-butyl ether
US5072049A (en) Process for the preparation of bis(4-hydroxyphenyl) sulfone
JPS56108791A (en) Continuous preparation of benzylidenesorbitol compound
JPH0345054B2 (en)
JPS6122038A (en) Production of unsaturated acetal
JPH0210140B2 (en)
JPH0780800B2 (en) Method for producing propylene glycol tert-butyl ether