MY130941A - Preparation of n- butyl alkyl ethers - Google Patents

Preparation of n- butyl alkyl ethers

Info

Publication number
MY130941A
MY130941A MYPI97004283A MYPI9704283A MY130941A MY 130941 A MY130941 A MY 130941A MY PI97004283 A MYPI97004283 A MY PI97004283A MY PI9704283 A MYPI9704283 A MY PI9704283A MY 130941 A MY130941 A MY 130941A
Authority
MY
Malaysia
Prior art keywords
group
give
adduct
butyl alkyl
butadiene
Prior art date
Application number
MYPI97004283A
Inventor
Jurgen Kanand
Michael Roper
Original Assignee
Basf Ag
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 Basf Ag filed Critical Basf Ag
Publication of MY130941A publication Critical patent/MY130941A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01Preparation of ethers
    • C07C41/18Preparation of ethers by reactions not forming ether-oxygen bonds
    • C07C41/20Preparation of ethers by reactions not forming ether-oxygen bonds by hydrogenation of carbon-to-carbon double or triple bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01Preparation of ethers
    • C07C41/32Preparation of ethers by isomerisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/48Preparation of compounds having groups
    • C07C41/50Preparation of compounds having groups by reactions producing groups
    • C07C41/54Preparation of compounds having groups by reactions producing groups by addition of compounds to unsaturated carbon-to-carbon bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

N-BUTYL ALKYL ETHERS ARE PREPARED BY A) REACTING 1,3-BUTADIENE OR A BUTADIENE-CONTAINING HYDROCARBON MIXTURE WITH AN ALCOHOL OF THE FORMULA I WHERE THE RADICAL R IS A C2-C20-ALKYL, ALKENYL, CYCLOALKYL OR CYCLOALKENYL GROUP, EACH OF WHICH MAY BE UNSUBSTITUTED OR SUBSTITUTED BY 1 OR 2 CL-C10-ALKOXY OR HYDROXY GROUPS, A C6-C10-ARYL GROUP OR A C7-C11-ARALKYL GROUP OR THE METHYL GROUP, AT ELEVATED TEMPERATURE AND ELEVATED PRESSURE IN THE PRESENCE OF A BRÖNSTED ACID OR IN THE PRESENCE OF A COMPLEX OF AN ELEMENT FROM GROUP IB, VIIB OR VIIIB OF THE PERIODIC TABLE OF THE ELEMENTS WITH PHOSPHORUSOR NITROGEN-CONTAINING LIGANDS TO GIVE A MIXTURE OF ADDUCTS OF THE FORMULAE II AND III B) SEPARATING THE ISOMERS,C) ISOMERIZING THE ADDUCT III TO GIVE THE ADDUCT II AND D) HYDROGENATING THE ADDUCT II IN THE LIQUID PHASE IN THE PRESENCE OF A HOMOGENEOUS OR HETEROGENEOUS TRANSITION METAL CATALYST OR IN THE GAS PHASE IN THE PRESENCE OF A HETEROGENEOUS TRANSITION METAL-CONTAINING CATALYST TO GIVE AN N-BUTYL ALKYL ETHER OF THE FORMULA IV.
MYPI97004283A 1996-09-17 1997-09-16 Preparation of n- butyl alkyl ethers MY130941A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19637895A DE19637895A1 (en) 1996-09-17 1996-09-17 Process for the preparation of n-butyl alkyl ethers

Publications (1)

Publication Number Publication Date
MY130941A true MY130941A (en) 2007-07-31

Family

ID=7805910

Family Applications (1)

Application Number Title Priority Date Filing Date
MYPI97004283A MY130941A (en) 1996-09-17 1997-09-16 Preparation of n- butyl alkyl ethers

Country Status (16)

Country Link
EP (1) EP0931046B1 (en)
JP (1) JP2001500868A (en)
KR (1) KR20000036150A (en)
CN (1) CN1232444A (en)
AT (1) ATE202550T1 (en)
AU (1) AU4300297A (en)
BR (1) BR9711485A (en)
CA (1) CA2265494A1 (en)
CZ (1) CZ85399A3 (en)
DE (2) DE19637895A1 (en)
ES (1) ES2160342T3 (en)
ID (1) ID18558A (en)
MY (1) MY130941A (en)
NO (1) NO991267L (en)
TW (1) TW372957B (en)
WO (1) WO1998012164A2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19838449A1 (en) * 1998-08-25 2000-03-02 Basf Ag Process for the separation of 1,3-butadiene and water from mixtures containing 1,3-butadiene, 1-n-butoxybutene-2, 3-n-butoxybutene-1, n-butanol, di-n-butyl ether and water
GB9823980D0 (en) * 1998-11-02 1998-12-30 Bp Chem Int Ltd A process for making n-butyl ethers of glycols
KR101363208B1 (en) * 2011-11-29 2014-02-13 롯데케미칼 주식회사 Selective alkylation method of diene compounds having 4 to 5 carbon atoms
GB201818905D0 (en) * 2018-11-20 2019-01-02 Bp Plc Process for making ethers via enol ethers
CN109529906B (en) * 2018-12-25 2021-06-15 西安近代化学研究所 Catalyst for synthesizing 1,1,2,3,3, 3-hexafluoropropyl methyl ether and preparation method thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3670032A (en) * 1969-03-19 1972-06-13 Exxon Research Engineering Co Preparation of unsaturated alcohols and ethers
US4843180A (en) * 1986-11-13 1989-06-27 The Dow Chemical Company Preparation of ethers
DE4400837A1 (en) * 1994-01-14 1995-07-20 Basf Ag Process for the preparation of n-butyraldehyde and / or n-butanol

Also Published As

Publication number Publication date
KR20000036150A (en) 2000-06-26
CZ85399A3 (en) 1999-12-15
EP0931046B1 (en) 2001-06-27
WO1998012164A2 (en) 1998-03-26
NO991267D0 (en) 1999-03-16
JP2001500868A (en) 2001-01-23
EP0931046A2 (en) 1999-07-28
TW372957B (en) 1999-11-01
NO991267L (en) 1999-03-16
DE59703924D1 (en) 2001-08-02
AU4300297A (en) 1998-04-14
BR9711485A (en) 1999-08-24
ATE202550T1 (en) 2001-07-15
WO1998012164A3 (en) 1999-04-01
ES2160342T3 (en) 2001-11-01
ID18558A (en) 1998-04-16
CN1232444A (en) 1999-10-20
CA2265494A1 (en) 1998-03-26
DE19637895A1 (en) 1998-03-19

Similar Documents

Publication Publication Date Title
Shi et al. Palladium-catalyzed cyclizations of bromodialkenyl ethers and amines
Weyerstahl et al. Constituents of the essential oil of Myrtus communis L. from Iran
Creary et al. Diels-Alder approach to bicyclic. alpha.-hydroxy ketones. Facile ketol rearrangements of strained. alpha.-hydroxy ketones
Sandler Reactions of gem-dihalocyclopropanes with electrophilic reagents. Formation of allyl derivatives and (or) dienes
Marino et al. Regioselective reactions of organocuprates with cycloalkene epoxides
de Oliveira Dias et al. Sustainable route to biomass-based amines: rhodium catalyzed hydroaminomethylation in green solvents
MY130941A (en) Preparation of n- butyl alkyl ethers
Rossi et al. Diastereoselective synthesis of (E)-alkenes and (E)-1, ω-dienes starting from diastereoisomeric mixtures of 1-bromo-1-alkenes: New syntheses of monounsaturated or bridged ring-ketal naturally occurring substances.
Davies et al. The rearrangements of allylic hydroperoxides derived from (+)-valencene
Tatsumi et al. Reactions of allylic compounds such as allyl alcohols, allyl ethers, and allylamines using trans-Mo (N2) 2 (Ph2PCH2CH2PPh2) 2
Pasto et al. Transfer Reactions Involving Boron. III. Hydroboration Studies with Enethiol Ethers
Hegedus et al. Palladium catalyzed allylic alkylation of olefins
Barluenga et al. C− C Bond Formation between Fischer Carbene Complexes and Allylic Alcohols by a [3, 4] Sigmatropic Rearrangement Promoted by a [1, 2] M (CO) 5 Shift
Shibuya et al. Phenolic components from leaf oil of Illicium anisatum L.
ID22905A (en) MAKING N-BUTIRALDEHIDA AND / OR N-BUTANOL
Trost et al. Regioselective cyclopropanation via unsymmetrical oxatrimethylenemethane palladium intermediates
Denis et al. Ligand-assisted catalysis: new active and selective nickel modified homogeneous catalysts for linear dimerization of butadiene
Chatani et al. Iridium-Catalyzed Reaction of Acetylene Hydrazones with a Hydrosilane and Carbon Monoxide. Synthesis of Nitrogen Heterocycles
Quick et al. Reactions of. alpha.-alkoxy-. alpha.,. beta.-unsaturated carbonyl compounds
Traylor et al. Stereoelectronic effects in arene exchange of (arene) tricarbonylchromium complexes: internal arene exchange and internal arene catalysis of external arene exchange
Sarma et al. Reductive removal of allylic functional groups by nickel boride
US5120868A (en) Catalyst system and process for the selective production of isoprenylalkyletheres from isoprene
US4721820A (en) Process for the isomerization of allylic ethers
Alcaide et al. Chromium Carbenes as Substrates in Cyclopropanation Reactions: 1, 4-vs 1, 2-Addition in the Reaction of Sulfur Ylides and. alpha.,. beta.-Unsaturated Alkoxychromium (0) Carbenes
Satoh et al. Syntheses of steroidal. PI.-allyl palladium chloride complexes.