IN2013MU01456A - - Google Patents

Info

Publication number
IN2013MU01456A
IN2013MU01456A IN1456MU2013A IN2013MU01456A IN 2013MU01456 A IN2013MU01456 A IN 2013MU01456A IN 1456MU2013 A IN1456MU2013 A IN 1456MU2013A IN 2013MU01456 A IN2013MU01456 A IN 2013MU01456A
Authority
IN
India
Prior art keywords
formula
nr1r2r3
represented
liquid compound
ionic liquid
Prior art date
Application number
Inventor
Pavankumar Aduri
Parasu Veera Uppara
Viswanath Kotra
Mangesh Sakhalkar
Vibhuti Dukhande
Original Assignee
Reliance Ind 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
Priority to IN1456MU2013 priority Critical patent/IN2013MU01456A/en
Priority to CN201480022227.4A priority patent/CN105142773B/en
Priority to BR112015026314A priority patent/BR112015026314A2/en
Priority to JP2016508294A priority patent/JP6356221B2/en
Priority to PCT/IN2014/000254 priority patent/WO2014178075A2/en
Priority to US14/784,742 priority patent/US9624248B2/en
Application filed by Reliance Ind Ltd filed Critical Reliance Ind Ltd
Priority to EP14791191.1A priority patent/EP2986371A4/en
Priority to KR1020157033045A priority patent/KR102012065B1/en
Priority to CA2909562A priority patent/CA2909562C/en
Priority to RU2015149264A priority patent/RU2654697C2/en
Publication of IN2013MU01456A publication Critical patent/IN2013MU01456A/en
Priority to SA515370018A priority patent/SA515370018B1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
    • C07F5/06—Aluminium compounds
    • C07F5/069—Aluminium compounds without C-aluminium linkages
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235—Nitrogen containing compounds
    • B01J31/0237—Amines
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0287—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing atoms other than nitrogen as cationic centre
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0287—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing atoms other than nitrogen as cationic centre
    • B01J31/0291—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing atoms other than nitrogen as cationic centre also containing elements or functional groups covered by B01J31/0201 - B01J31/0274
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0298—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature the ionic liquids being characterised by the counter-anions
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/04—Mixing
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F7/00—Compounds of aluminium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08—Catalytic processes
    • C07C2/26—Catalytic processes with hydrides or organic compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
    • C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
    • C07C2/66—Catalytic processes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
    • C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
    • C07C2/66—Catalytic processes
    • C07C2/68—Catalytic processes with halides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/86—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon
    • C07C2/861—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only halogen as hetero-atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
    • C07C211/62—Quaternary ammonium compounds
    • C07C211/63—Quaternary ammonium compounds having quaternised nitrogen atoms bound to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
    • C07C37/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms by condensation involving hydroxy groups of phenols or alcohols or the ether or mineral ester group derived therefrom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
    • C07C45/46—Friedel-Crafts reactions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/28—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/293—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/90—Antimony compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/20—Olefin oligomerisation or telomerisation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32—Addition reactions to C=C or C-C triple bonds
    • B01J2231/324—Cyclisations via conversion of C-C multiple to single or less multiple bonds, e.g. cycloadditions
    • B01J2231/326—Diels-Alder or other [4+2] cycloadditions, e.g. hetero-analogues
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/42—Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
    • B01J2231/4205—C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/06—Halogens; Compounds thereof
    • C07C2527/125—Compounds comprising a halogen and scandium, yttrium, aluminium, gallium, indium or thallium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated

Abstract

The present disclosure provides an ionic liquid compound of Formula (I) and its application in reactions such as alkylation, arylation, acylation, diels alder and oligomerization. [(NR1R2R3)iM1]n+[(M2Yk)L Xj]n- Formula I The present disclosure also provides a process for preparing the ionic liquid compound of Formula (I) which involves preparing an ionic salt complex represented by Formula [(NR1R2R3)iM1]n+[Xj]n- by mixing an amine represented by Formula NR1R2R3 and a metal salt represented by formula M1Xj; and mixing the ionic salt complex and a metal salt represented by formula M2¬Yk to obtain the ionic liquid compound.
IN1456MU2013 2013-04-19 2014-04-21 IN2013MU01456A (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
CN201480022227.4A CN105142773B (en) 2013-04-19 2014-04-21 Ion liquid compound
BR112015026314A BR112015026314A2 (en) 2013-04-19 2014-04-21 ionic liquid compound
JP2016508294A JP6356221B2 (en) 2013-04-19 2014-04-21 Ionic liquid compounds
PCT/IN2014/000254 WO2014178075A2 (en) 2013-04-19 2014-04-21 Ionic liquid compound
US14/784,742 US9624248B2 (en) 2013-04-19 2014-04-21 Ionic liquid compound
IN1456MU2013 IN2013MU01456A (en) 2013-04-19 2014-04-21
EP14791191.1A EP2986371A4 (en) 2013-04-19 2014-04-21 Ionic liquid compound
KR1020157033045A KR102012065B1 (en) 2013-04-19 2014-04-21 Ionic liquid compound
CA2909562A CA2909562C (en) 2013-04-19 2014-04-21 Ionic liquid compound for catalysis of chemical reactions
RU2015149264A RU2654697C2 (en) 2013-04-19 2014-04-21 Ionic liquid
SA515370018A SA515370018B1 (en) 2013-04-19 2015-10-18 Ionic liquid compound

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IN1456MU2013 IN2013MU01456A (en) 2013-04-19 2014-04-21

Publications (1)

Publication Number Publication Date
IN2013MU01456A true IN2013MU01456A (en) 2015-04-17

Family

ID=51844060

Family Applications (1)

Application Number Title Priority Date Filing Date
IN1456MU2013 IN2013MU01456A (en) 2013-04-19 2014-04-21

Country Status (11)

Country Link
US (1) US9624248B2 (en)
EP (1) EP2986371A4 (en)
JP (1) JP6356221B2 (en)
KR (1) KR102012065B1 (en)
CN (1) CN105142773B (en)
BR (1) BR112015026314A2 (en)
CA (1) CA2909562C (en)
IN (1) IN2013MU01456A (en)
RU (1) RU2654697C2 (en)
SA (1) SA515370018B1 (en)
WO (1) WO2014178075A2 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20170203286A1 (en) * 2014-07-10 2017-07-20 Reliance Industries Limited Ionic liquid, adduct and methods thereof
WO2016071871A1 (en) * 2014-11-07 2016-05-12 Reliance Industries Limited Ionic liquid compound based transalkylation process
CN106582844B (en) * 2015-10-19 2019-04-19 中国石油化工股份有限公司 A kind of aromatic alkylation catalysts composition and application
US10246395B2 (en) 2016-12-19 2019-04-02 The Board Of Trustees Of The University Of Alabama Methods of acylation with an ionic liquid catalyzing medium
US11045833B2 (en) 2017-02-03 2021-06-29 Massachusetts Institute Of Technology Task specific ionic liquid-impregnated polymeric surface coatings for antibacterial, antifouling, and metal scavenging activity
WO2020121154A1 (en) * 2018-12-09 2020-06-18 Reliance Industries Limited Process for preparing linear alkyl benzene
CN112403515B (en) * 2020-12-04 2022-09-02 江苏棋成化工有限公司 Asymmetric bimetal dication ionic liquid catalyst, preparation method and application thereof
CN113842775A (en) * 2021-10-14 2021-12-28 青岛科技大学 Method for removing hydrogen sulfide by liquid-phase catalytic oxidation

Family Cites Families (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3104267A (en) 1960-09-12 1963-09-17 Sun Oil Co Preparing of long chain alkyl aromatic hydrocarbons
US3269996A (en) * 1962-09-18 1966-08-30 Exxon Research Engineering Co Three-component polymerization catalysts containing coordination complexes
US3249650A (en) 1963-10-18 1966-05-03 Universal Oil Prod Co Isoparaffin alkylation process
US3346657A (en) 1964-12-30 1967-10-10 Gulf Research Development Co Process for alkylating aromatic hydrocarbons using supported heteropoly acid catalyst
US3560587A (en) 1969-04-14 1971-02-02 Universal Oil Prod Co Hydrogen fluoride alkylation with reaction cooler and reaction soaker vessels
US3494971A (en) 1969-04-18 1970-02-10 Universal Oil Prod Co Process for the production of a monoalkylated aromatic hydrocarbon
US3713615A (en) 1971-01-08 1973-01-30 Universal Oil Prod Co Alkylation fractionator
US3686354A (en) 1971-02-04 1972-08-22 Universal Oil Prod Co High octane paraffinic motor fuel production
US3950448A (en) 1975-02-24 1976-04-13 Universal Oil Products Company Detergent-grade alkylate production
IT1038893B (en) 1975-06-11 1979-11-30 Liquichimica Spa PROCESS FOR THE PREPARATION OF ALKYLBENZOLES
US4239931A (en) 1979-11-05 1980-12-16 Uop Inc. HF Alkylatior process
US4368342A (en) 1980-12-22 1983-01-11 Shell Oil Company Benzene alkylation process
US4358628A (en) 1981-06-26 1982-11-09 Shell Oil Company Alkylation of benzene compounds with detergent range olefins
US4513156A (en) 1984-04-16 1985-04-23 Mobil Oil Corporation Olefin oligomerization using extracted feed for production of heavy hydrocarbons
US4973780A (en) 1988-04-27 1990-11-27 Lummus Crest, Inc. Alkylation of benzene in a moving bed
US5196624A (en) 1990-04-27 1993-03-23 Chevron Research And Technology Company Detergent grade to C10 to C28 olefins, (C10 to C28 alkyl)benzenes and C10 to C28 alkyl) benzene sulfonates and process for preparing same using a phosphine containing catalyst
US5196574A (en) 1991-12-23 1993-03-23 Uop Detergent alkylation process using a fluorided silica-alumina
US5344997A (en) 1991-12-23 1994-09-06 Uop Alkylation of aromatics using a fluorided silica-alumina catalyst
US5334793A (en) 1992-07-27 1994-08-02 Uop Increasing catalyst life and improving product linearity in the alkylation of aromatics with linear olefins
US5284993A (en) 1992-09-21 1994-02-08 Phillips Petroleum Company Alkylation catalyst regeneration
IT1255512B (en) 1992-09-24 1995-11-09 Pierino Radici IMPROVED PROCESS FOR THE PRODUCTION OF LINEAR ALCHYLBENZENES
US5777187A (en) 1996-02-08 1998-07-07 Huntsman Petrochemical Corporation Two-step process for alkylation of benzene to form linear alkylbenzenes
US6133492A (en) 1996-02-08 2000-10-17 Huntsman Petrochemical Corporation Alkylation of benzene to form linear alkylbenzenes using fluorine-containing mordenites
US5847254A (en) 1996-02-08 1998-12-08 Huntsman Petrochemical Corporation Alkylation of benzene to form linear alkylbenzenes using fluorine-containing mordenites
US5731101A (en) * 1996-07-22 1998-03-24 Akzo Nobel Nv Low temperature ionic liquids
US5824832A (en) 1996-07-22 1998-10-20 Akzo Nobel Nv Linear alxylbenzene formation using low temperature ionic liquid
US5894076A (en) 1997-05-12 1999-04-13 Catalytic Distillation Technologies Process for alkylation of benzene
WO1999003163A1 (en) 1997-07-10 1999-01-21 Akzo Nobel Inc. Alkylation reaction using supported ionic liquid catalyst composition and catalyst composition
EP0989134A1 (en) * 1998-09-11 2000-03-29 Akzo Nobel N.V. Process for the in situ preparation of an ionic liquid
AU1672100A (en) * 1999-01-15 2000-08-01 Bp Chemicals Limited Ionic liquid catalyst for alkylation
CN1184284C (en) * 2002-01-18 2005-01-12 石油大学(北京) Method of utilizing ionic liquid as catalyst in preparing alkylated oil
WO2003089389A2 (en) * 2002-04-22 2003-10-30 Chevron Phillips Chemical Company Lp Method for manufacturing ionic liquid catalysts
CN1203032C (en) 2002-11-12 2005-05-25 石油大学(北京) Preparing method for alkylate agent using compound ion as catalyst
CA2518597C (en) 2003-03-10 2012-01-17 Sasol Technology (Proprietary) Limited Production of linear alkyl benzene
US8329603B2 (en) 2003-09-16 2012-12-11 Uop Llc Isoparaffin-olefin alkylation
US8524965B2 (en) * 2005-12-21 2013-09-03 Chevron Oronite Company Llc Method of making an alkylated aromatic using acidic ionic liquid catalyst
US7655824B2 (en) 2006-10-30 2010-02-02 Uop Llc Processes for producing alkylbenzenes over solid acid catalyst at low benzene to olefin ratios and low heavies make
CN101619010B (en) * 2009-07-17 2013-04-03 中国石油大学(北京) Method for regenerating and maintaining activity of ionic liquid catalyst and method for producing alkylate
US20110118517A1 (en) 2009-11-19 2011-05-19 Uop Llc Manufacturing Process for Branched and Linear Alkylated Benzene as Precursor for Enhanced Oil Recovery Surfactant
US9126184B2 (en) 2009-12-16 2015-09-08 Uop Llc Detergent alkylation using a rare earth exchanged catalyst
ES2522545T3 (en) * 2010-02-11 2014-11-17 Basf Se Process for obtaining m-substituted alkyl toluenes by isomerization with ionic liquids as catalysts
EP2593213A4 (en) * 2010-06-29 2014-08-27 Reliance Ind Ltd Ionic fluids
US20120169298A1 (en) 2011-01-05 2012-07-05 Boulder Ionics Corporation System and method for electrochemical device with metal containing ionic liquid electrolytes

Also Published As

Publication number Publication date
US20160060277A1 (en) 2016-03-03
RU2654697C2 (en) 2018-05-22
CN105142773B (en) 2018-05-18
JP6356221B2 (en) 2018-07-11
US9624248B2 (en) 2017-04-18
WO2014178075A3 (en) 2014-12-24
CA2909562A1 (en) 2014-11-06
JP2016516810A (en) 2016-06-09
RU2015149264A (en) 2017-05-24
KR20150145254A (en) 2015-12-29
SA515370018B1 (en) 2016-06-16
EP2986371A4 (en) 2017-02-08
BR112015026314A2 (en) 2017-07-25
KR102012065B1 (en) 2019-08-19
CA2909562C (en) 2019-07-30
EP2986371A2 (en) 2016-02-24
WO2014178075A2 (en) 2014-11-06
CN105142773A (en) 2015-12-09

Similar Documents

Publication Publication Date Title
SA515370018B1 (en) Ionic liquid compound
PH12017500833A1 (en) Synthesis of copanlisib and its dihydrochloride salt
IN2014CN03143A (en)
PH12015501960A1 (en) Processes for the preparation of an apoptosis-inducing agent
MX347882B (en) Improved process for preparing (3e,7e)-homofarnesol.
JO3487B1 (en) Synthesis of copanlisib and its dihydrochloride salt
MX2017009542A (en) Branched and linear chimeric compounds, polynucleotides, uses and methods for preparation thereof.
MX2013000009A (en) Process for the preparation of the l-arginine salt of perindopril.
BR112016008895A8 (en) methods for the formation of homoalicylic compounds by the reaction of cyclopropyl vinyl precursors with bronsted acid, and for the formation of ambrox
IN2014DN08777A (en)
IN2013CH04906A (en)
NZ742785A (en) Methods for preparing substituted 5,6-dihydro-6-phenylbenzo[f]isoquinolin-2-amine
MX2015013589A (en) Process and intermediates for the preparation of pregabalin.
WO2014141294A3 (en) An improved process for the synthesis of melphalan and the hydrochloride salt
GB2523674A (en) Compounds as inhibitor of DNA double-strand break repair, methods and applications thereof
MX2015015746A (en) Process for preparation of arformoterol of salt thereof.
IN2014DN07162A (en)
MX369174B (en) Process for preparing a compound.
MX2015011881A (en) Process for the preparation of 3,7-dimethylnonan-1-ol.
MX2015017747A (en) Process for producing 2-phenyl-1,3-benzoxazoles.
WO2015001565A3 (en) "an improved process for the preparation of 3-aryloxy-3- phenylpropylamine and salt thereof"
IN2013CH04635A (en)
IN2013MU02280A (en)
IN2013MU03144A (en)
IN2013MU01941A (en)