MX3189E - IMPROVED PROCESS TO OBTAIN ETERES - Google Patents

IMPROVED PROCESS TO OBTAIN ETERES

Info

Publication number
MX3189E
MX3189E MX002843U MX284375U MX3189E MX 3189 E MX3189 E MX 3189E MX 002843 U MX002843 U MX 002843U MX 284375 U MX284375 U MX 284375U MX 3189 E MX3189 E MX 3189E
Authority
MX
Mexico
Prior art keywords
reactant
inert hydrocarbon
weight
ether
reaction mixture
Prior art date
Application number
MX002843U
Other languages
Spanish (es)
Inventor
Edward Lauwrence Cole
Sheldon Herbstman
John Thomas Nolan Jr
Original Assignee
Texaco Development 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 Texaco Development Corp filed Critical Texaco Development Corp
Publication of MX3189E publication Critical patent/MX3189E/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01Preparation of ethers
    • C07C41/05Preparation of ethers by addition of compounds to unsaturated compounds
    • C07C41/06Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

La presente invención se refiere a proceso mejorado para obtención de un éter, mediante la reación a una temperatura de 37.7°C a 149°C, y una presión de 3.5 kilos a 52.50 kilos por cm2 manométricos, de un alcohol soluble en agua, como primer reactante y una olefina o alcohol insoluble en agua, como segundo reactante, en una relación molar de primer reactante a segundo reactante de 1-2:1 a 4.0:1 en la presencia de una resina sólida como catalizador de eterificación, formando de este modo, una mezcla de reacción que incluye el primer reactante no-reaccionado, y el éter del producto que tiene radicales del primer reactante y el segundo reactante caracterizado porque las mejoras comprenden poner a reaccionar en un solvente de hidrocarburo inerte, que tiene de 3 a 4 átomos de carbono, el catalizador que comprende de 0.1 a 10 en peso (base seca) de los reactantes y el hidrocarburo inerte, y la relación ponderal del hidrocarburo inerte para cada 100 partes por peso del reactante y poniendo en contacto la mezcla de reacción que contiene el solvente de hidrocarburo inerte con un extractante acuoso formado con ello un extracto acuoso que tiene el primer reactante y un finado que contiene el hidrocarburo inerte y el éter del producto recuperando el refinado.(ver gaceta).The present invention refers to an improved process for obtaining an ether, by reacting at a temperature of 37.7 ° C to 149 ° C, and a pressure of 3.5 kilos to 52.50 kilos per cm2 gauge, of a water soluble alcohol, such as first reactant and a water-insoluble olefin or alcohol, as the second reactant, in a molar ratio of first reactant to second reactant of 1-2: 1 to 4.0: 1 in the presence of a solid resin as an etherification catalyst, thereby forming Thus, a reaction mixture that includes the first unreacted reactant, and the product ether that has radicals from the first reactant and the second reactant characterized in that the improvements include reacting in an inert hydrocarbon solvent, which has from 3 to 4 carbon atoms, the catalyst comprising 0.1 to 10 by weight (dry basis) of the reactants and the inert hydrocarbon, and the weight ratio of the inert hydrocarbon for each 100 parts by weight of the reactant and setting e I contacted the reaction mixture containing the inert hydrocarbon solvent with an aqueous extractant, thereby formed an aqueous extract having the first reactant and a product containing the inert hydrocarbon and the product ether recovering the raffinate (see gazette).

MX002843U 1974-12-02 1975-11-28 IMPROVED PROCESS TO OBTAIN ETERES MX3189E (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US52897074A 1974-12-02 1974-12-02

Publications (1)

Publication Number Publication Date
MX3189E true MX3189E (en) 1980-06-23

Family

ID=24107977

Family Applications (1)

Application Number Title Priority Date Filing Date
MX002843U MX3189E (en) 1974-12-02 1975-11-28 IMPROVED PROCESS TO OBTAIN ETERES

Country Status (15)

Country Link
JP (1) JPS5168512A (en)
AR (1) AR218609A1 (en)
AT (1) AT348497B (en)
BE (1) BE836051A (en)
BR (1) BR7507887A (en)
DE (1) DE2547380A1 (en)
ES (1) ES443080A1 (en)
FR (1) FR2293411A1 (en)
GB (1) GB1473263A (en)
IN (1) IN143386B (en)
IT (1) IT1051014B (en)
MX (1) MX3189E (en)
NL (1) NL7513964A (en)
PH (1) PH11937A (en)
SE (1) SE7513302L (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PH12545A (en) * 1975-06-06 1979-06-07 Texaco Development Corp Method for preparation of ethers
JPS5714547A (en) * 1980-06-11 1982-01-25 Inst Francais Du Petrole Manufacture of methyl-tert-butyl ether from methanol and isobutene
DE3024147C2 (en) 1980-06-27 1983-05-05 Edeleanu Gmbh, 6000 Frankfurt Process for the separation of the reaction products obtained in the etherification of lower i-olefins with methanol
DE3150755A1 (en) * 1981-12-22 1983-06-30 Deutsche Texaco Ag, 2000 Hamburg "METHOD FOR SEPARATING METHANOL FROM THE REACTION PRODUCTS INCLUDING METHANOL FROM C (ARROW DOWN) 4 (ARROW DOWN) TO C (ARROW DOWN) 7 (ARROW DOWN) 7 (ARROW DOWN)"
FR2565991B1 (en) * 1984-06-18 1986-10-03 Inst Francais Du Petrole PROCESS FOR THE VALORIZATION OF OLEFINIC ESSENCES BY ETHERIFICATION
DE3435936A1 (en) * 1984-09-29 1986-04-10 Linde Ag, 6200 Wiesbaden METHOD AND DEVICE FOR PRODUCING AETHER
US5329051A (en) * 1992-12-30 1994-07-12 Phillips Petroleum Company Ether recovery
DE4445635A1 (en) * 1994-12-21 1996-06-27 Veba Oel Ag Process for the preparation of polyol alkyl ethers

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB954197A (en) * 1959-05-04 1964-04-02 Sinclair Refining Co Recovery of tertiary olefins
DE1224294B (en) * 1961-01-09 1966-09-08 Bayer Ag Process for the production of tertiary butyl alkyl ethers
FR2012552A1 (en) * 1968-07-09 1970-03-20 Shell Int Research Tertiary olefins prodn and purification - using an ion-exchange catalyst
BE791661A (en) * 1971-11-22 1973-05-21 Sun Oil Co Pennsylvania MANUFACTURE OF GASOLINE COMPOUNDS CONTAINING METHYL-2-METHOXY-2-PROPANE
BE793163A (en) * 1971-12-22 1973-06-21 Sun Oil Co Pennsylvania ETHERS DRYING PROCESS

Also Published As

Publication number Publication date
DE2547380C2 (en) 1989-10-05
NL7513964A (en) 1976-06-04
BE836051A (en) 1976-05-28
ATA833875A (en) 1978-07-15
PH11937A (en) 1978-09-15
BR7507887A (en) 1976-09-08
AR218609A1 (en) 1980-06-30
IT1051014B (en) 1981-04-21
FR2293411B1 (en) 1980-05-16
ES443080A1 (en) 1977-04-01
AT348497B (en) 1979-02-26
DE2547380A1 (en) 1976-08-12
FR2293411A1 (en) 1976-07-02
JPS5168512A (en) 1976-06-14
GB1473263A (en) 1977-05-11
SE7513302L (en) 1976-06-03
IN143386B (en) 1977-11-12

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