NL6514991A - - Google Patents

Info

Publication number: NL6514991A
Authority: NL; Netherlands
Prior art keywords: vinyl ether; ether; acetal; hydroxy compound; methyl
Prior art date: 1964-11-19

Application number

NL6514991A

Other languages

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.)

1964-11-19

Filing date

1965-11-18

Publication date

1966-05-20

1965-11-18 Application filed filed Critical

1966-05-20 Publication of NL6514991A publication Critical patent/NL6514991A/xx

Links

QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 abstract 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 3
JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 abstract 3
-1 cycloaliphatic Chemical group 0.000 abstract 3
150000002440 hydroxy compounds Chemical class 0.000 abstract 3
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 abstract 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract 2
150000001241 acetals Chemical class 0.000 abstract 2
239000003054 catalyst Substances 0.000 abstract 2
238000006243 chemical reaction Methods 0.000 abstract 2
125000000623 heterocyclic group Chemical group 0.000 abstract 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 abstract 2
KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 abstract 2
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 abstract 2
150000003839 salts Chemical class 0.000 abstract 2
238000005690 transetherification reaction Methods 0.000 abstract 2
OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 abstract 1
KIELJSVPUISYCI-UHFFFAOYSA-N 2-methyl-1-[1-(2-methylpropoxy)ethoxy]propane Chemical compound CC(C)COC(C)OCC(C)C KIELJSVPUISYCI-UHFFFAOYSA-N 0.000 abstract 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 abstract 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
125000001931 aliphatic group Chemical group 0.000 abstract 1
229910001508 alkali metal halide Inorganic materials 0.000 abstract 1
150000008045 alkali metal halides Chemical class 0.000 abstract 1
125000003342 alkenyl group Chemical group 0.000 abstract 1
125000000217 alkyl group Chemical group 0.000 abstract 1
125000000304 alkynyl group Chemical group 0.000 abstract 1
125000003710 aryl alkyl group Chemical group 0.000 abstract 1
125000003118 aryl group Chemical group 0.000 abstract 1
WXNOJTUTEXAZLD-UHFFFAOYSA-L benzonitrile;dichloropalladium Chemical compound Cl[Pd]Cl.N#CC1=CC=CC=C1.N#CC1=CC=CC=C1 WXNOJTUTEXAZLD-UHFFFAOYSA-L 0.000 abstract 1
230000015572 biosynthetic process Effects 0.000 abstract 1
239000006227 byproduct Substances 0.000 abstract 1
239000008139 complexing agent Substances 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
150000001896 cresols Chemical class 0.000 abstract 1
238000002425 crystallisation Methods 0.000 abstract 1
230000008025 crystallization Effects 0.000 abstract 1
125000004122 cyclic group Chemical group 0.000 abstract 1
125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
125000000753 cycloalkyl group Chemical group 0.000 abstract 1
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 abstract 1
238000004821 distillation Methods 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
238000011065 in-situ storage Methods 0.000 abstract 1
229910052741 iridium Inorganic materials 0.000 abstract 1
150000002576 ketones Chemical class 0.000 abstract 1
229910052744 lithium Inorganic materials 0.000 abstract 1
229910052762 osmium Inorganic materials 0.000 abstract 1
229910052763 palladium Inorganic materials 0.000 abstract 1
KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 1
PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 abstract 1
150000002989 phenols Chemical class 0.000 abstract 1
229910052697 platinum Inorganic materials 0.000 abstract 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
239000000047 product Substances 0.000 abstract 1
229910052703 rhodium Inorganic materials 0.000 abstract 1
229910052707 ruthenium Inorganic materials 0.000 abstract 1
239000002904 solvent Substances 0.000 abstract 1
238000000638 solvent extraction Methods 0.000 abstract 1
125000001424 substituent group Chemical group 0.000 abstract 1
125000001174 sulfone group Chemical group 0.000 abstract 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
150000003739 xylenols Chemical class 0.000 abstract 1

Classifications

- 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
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D19/00—Degasification of liquids
- B01D19/02—Foam dispersion or prevention
- B01D19/04—Foam dispersion or prevention by addition of chemical substances
- B01D19/0404—Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
- 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
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/08—Halides
- 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
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
- B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
- B01J31/223—At least two oxygen atoms present in one at least bidentate or bridging ligand
- B01J31/2239—Bridging ligands, e.g. OAc in Cr2(OAc)4, Pt4(OAc)8 or dicarboxylate ligands
- 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
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
- B01J31/28—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of the platinum group metals, iron group metals or copper
- B01J31/30—Halides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/14—Preparation of ethers by exchange of organic parts on the ether-oxygen for other organic parts, e.g. by trans-etherification
- 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
- 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
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- 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
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/824—Palladium
- 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
- B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Inorganic Chemistry (AREA)
Health & Medical Sciences (AREA)
Toxicology (AREA)
Dispersion Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NL6514991A 1964-11-19 1965-11-18 NL6514991A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB47173/64A GB1105956A (en)	1964-11-19	1964-11-19	Process for the production of vinyl ethers

Publications (1)

Publication Number	Publication Date
NL6514991A true NL6514991A (fr)	1966-05-20

Family

ID=10444011

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL6514991A NL6514991A (fr)	1964-11-19	1965-11-18

Country Status (4)

Country	Link
DE (1)	DE1275532B (fr)
FR (1)	FR2049783A5 (fr)
GB (1)	GB1105956A (fr)
NL (1)	NL6514991A (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4950420A (en) *	1988-08-31	1990-08-21	Nalco Chemical Company	Antifoam/defoamer composition
DE102012105879A1 (de)	2012-07-02	2014-01-02	Oxea Gmbh	Verfahren zur Herstellung von Isononylderivaten

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2579412A (en) *	1950-03-02	1951-12-18	Du Pont	Reaction of vinyl ethers with hydroxy compounds

1964
- 1964-11-19 GB GB47173/64A patent/GB1105956A/en not_active Expired
1965
- 1965-11-18 NL NL6514991A patent/NL6514991A/xx unknown
- 1965-11-19 DE DEJ29414A patent/DE1275532B/de active Pending
1970
- 1970-06-02 FR FR7020143A patent/FR2049783A5/fr not_active Expired

Also Published As

Publication number	Publication date
DE1275532B (de)	1968-08-22
FR2049783A5 (en)	1971-03-26
GB1105956A (en)	1968-03-13

Publication	Publication Date	Title
McKeon et al.	1972	The palladium (II) catalyzed vinyl interchange reaction—II
GB1234641A (fr)	1971-06-09
Bryson	1973	Convenient preparation of tetrahydrofurylidene acetates
GB1105956A (en)	1968-03-13	Process for the production of vinyl ethers
US3173933A (en)	1965-03-16	Oxidation of alcohols and ethers to carbonyl containing compounds
GB1361952A (en)	1974-07-30	Production of methylene and oxymethylene dicarboxylic acid esters
Saxton	1965	Alkaloids of Haplophyton cimicidum
Bax et al.	1971	Mixed carboxylic anhydrides: Part IX. Synthesis of alkyl thiolformates
ES309337A1 (es)	1965-12-16	Procedimiento de obtencion de acetato de alilo
GB1111714A (en)	1968-05-01	Process for the production of ethylenic compounds
US2038609A (en)	1936-04-28	Compounds containing a mercaptide group and method of producing same
GB1293839A (en)	1972-10-25	Potassium titanyl oxalate
GB1278353A (en)	1972-06-21	Preparation of dicarboxylic acids
SU100296A1 (ru)	1955-09-05	Способ защиты хлоргидрина стирола от разложени , вызываемого присутствием железных солей, металлического железа или металлических сплавов, содержащих железо
GB1359372A (en)	1974-07-10	Preparation of 1,1,2-trimethoxyethane and o-acetic acid methyl ester
GB1063435A (en)	1967-03-30	Production of vinyl esters
O'Leary et al.	1933	Reactions and properties of boron fluoride in methyl alcohol
SU215961A1 (ru)	1968-04-11	Способ получени замещенных в дре винилариловых эфиров
US3641162A (en)	1972-02-08	Production of ethers
GB1131285A (en)	1968-10-23	Ethers of propargyl alcohol
US2634267A (en)	1953-04-07	Penicillin salt of dimethylaminoacetoxy-dibenzylpropane
ES293280A1 (es)	1964-01-01	Procedimiento de preparación de derivados 1-hidroximetil desacetilamino colchícicos
GB824520A (en)	1959-12-02	Improvements in the production of acrylic acid esters
Phillips et al.	1963	Synthesis of Deuteriated Methyl Benzoates and Dimethyl Phthalates
JPS5551037A (en)	1980-04-14	Preparation of dicarboxylic acid by carbonylation reaction of lactones