FR2288747A1 - Tungsten cpds. contg. silanol gps. - and tungsten complex cpds. contg. ligands used as allyl alcohol isomerisation catalysts - Google Patents
Tungsten cpds. contg. silanol gps. - and tungsten complex cpds. contg. ligands used as allyl alcohol isomerisation catalystsInfo
- Publication number
- FR2288747A1 FR2288747A1 FR7512501A FR7512501A FR2288747A1 FR 2288747 A1 FR2288747 A1 FR 2288747A1 FR 7512501 A FR7512501 A FR 7512501A FR 7512501 A FR7512501 A FR 7512501A FR 2288747 A1 FR2288747 A1 FR 2288747A1
- Authority
- FR
- France
- Prior art keywords
- cpds
- contg
- tungsten
- pref
- silanol
- 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.)
- Withdrawn
Links
- 229910052721 tungsten Inorganic materials 0.000 title abstract 4
- 239000003054 catalyst Substances 0.000 title abstract 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 title 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 title 2
- 239000010937 tungsten Substances 0.000 title 2
- 238000006317 isomerization reaction Methods 0.000 title 1
- 239000003446 ligand Substances 0.000 title 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 title 1
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 abstract 4
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 3
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 abstract 1
- 239000005792 Geraniol Substances 0.000 abstract 1
- GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 abstract 1
- 150000004808 allyl alcohols Chemical class 0.000 abstract 1
- 229910052785 arsenic Inorganic materials 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 229910052797 bismuth Inorganic materials 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 229940113087 geraniol Drugs 0.000 abstract 1
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/06—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms
- C07C403/08—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms by hydroxy groups
-
- 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
- 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
- B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
-
- 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
-
- 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
- B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/56—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by isomerisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic
- C07C35/06—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a five-membered rings
-
- 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
- C07F11/00—Compounds containing elements of Groups 6 or 16 of the Periodic Table
- C07F11/005—Compounds containing elements of Groups 6 or 16 of the Periodic Table compounds without a metal-carbon linkage
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0836—Compounds with one or more Si-OH or Si-O-metal linkage
-
- 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
- B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
- B01J2231/52—Isomerisation 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
- B01J2531/60—Complexes comprising metals of Group VI (VIA or VIB) as the central metal
- B01J2531/66—Tungsten
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/09—Geometrical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/10—Systems containing only non-condensed rings with a five-membered ring the ring being unsaturated
-
- 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
- C07C2601/14—The ring being saturated
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
Abstract
New W complex cpds. have general formula WO(OR1) (OR2)(OR3)(OR4) nL, (I), (where R1,R2, R3 and R4 are opt. substd. hydrocarbyl or -SiR5R6R7, in which R5, R6, R7 are opt. substd. hydrocarbyl, and 2 or more of R1, R2, R3 and R4 can form a cyclic structure together with adjoining W and O atoms; L is a mono-or poly-dentated ligan contg. a typical element of Gp. V of periodic system, pref. N, P, As or Bi, via which it is coordinatively bonded with W, and n is 1 to no. of W atoms bonded to L). New W cpds. have general formula WO(OR1)(OR2)(OR3)(OR4), (II), in which at least one of R1, R2, R3 and R4 is -SiR5R6R7. (I) and/or (II) are pref. used as catalysts for isomerising allyl alcohols having formula R11R12COH-CR13=CR14R15 (III), (where R11 to R15 are H or opt. substd. hydrocarbyl), pref. linalol, to R11R12C=CR13-CR14R15OH (IV), pref. geraniol and/or nerol, or vice-versa.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP49045353A JPS5747890B2 (en) | 1974-04-22 | 1974-04-22 | |
JP49045350A JPS5826357B2 (en) | 1974-04-22 | 1974-04-22 | Tungsten Sakuka Gobutsu Oyobi Sonoso Seibutsu |
JP49045351A JPS5740813B2 (en) | 1974-04-22 | 1974-04-22 | |
JP49045354A JPS5826358B2 (en) | 1974-04-22 | 1974-04-22 | Tungsten bag |
Publications (1)
Publication Number | Publication Date |
---|---|
FR2288747A1 true FR2288747A1 (en) | 1976-05-21 |
Family
ID=27461686
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7512501A Withdrawn FR2288747A1 (en) | 1974-04-22 | 1975-04-22 | Tungsten cpds. contg. silanol gps. - and tungsten complex cpds. contg. ligands used as allyl alcohol isomerisation catalysts |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE2516698A1 (en) |
FR (1) | FR2288747A1 (en) |
IT (1) | IT1037568B (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2189014T3 (en) * | 1997-02-25 | 2003-07-01 | Basf Ag | PROCEDURE FOR INSOMERIZATION OF ALILIC ALCOHOLS. |
DE19958603A1 (en) * | 1999-12-06 | 2001-06-07 | Basf Ag | Process for the isomerization of allyl alcohols |
DE10046865A1 (en) * | 2000-09-20 | 2002-03-28 | Basf Ag | New tungstyl peroxide complexes useful as catalysts for isomerizing allylic alcohols, e.g. geraniol |
DE10160146A1 (en) | 2001-12-07 | 2003-06-18 | Basf Ag | Process for the isomerization of allylic alcohols |
DE10160147A1 (en) | 2001-12-07 | 2003-06-18 | Basf Ag | Process for the isomerization of allylic alcohols |
EP2657216B1 (en) | 2012-04-27 | 2014-06-25 | Symrise AG | Method for converting farnesol to nerolidol in the presence of alpha-bisabolol |
CN116003219A (en) * | 2022-12-21 | 2023-04-25 | 江苏宏邦化工科技有限公司 | Method for synthesizing nerol geraniol by synergistic catalysis |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1811517A1 (en) * | 1967-11-28 | 1969-07-17 | Rhone Poulenc Sa | Process for the production of ethylenic carbonyl compounds |
-
1975
- 1975-04-16 DE DE19752516698 patent/DE2516698A1/en active Pending
- 1975-04-21 IT IT22605/75A patent/IT1037568B/en active
- 1975-04-22 FR FR7512501A patent/FR2288747A1/en not_active Withdrawn
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1811517A1 (en) * | 1967-11-28 | 1969-07-17 | Rhone Poulenc Sa | Process for the production of ethylenic carbonyl compounds |
Non-Patent Citations (1)
Title |
---|
EXBK/65 * |
Also Published As
Publication number | Publication date |
---|---|
IT1037568B (en) | 1979-11-20 |
DE2516698A1 (en) | 1975-10-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SE403077B (en) | DEVICE FOR CONVERSION OF A CHAIR SEAT, IN PARTICULAR A VEHICLE SEAT, HEIGHT AND SLOPE | |
BE809656A (en) | CHAIR BODY | |
CA975300A (en) | Axial flow turbine structure | |
BE821656A (en) | FUEL CONTAINING WAX | |
FR2288747A1 (en) | Tungsten cpds. contg. silanol gps. - and tungsten complex cpds. contg. ligands used as allyl alcohol isomerisation catalysts | |
SE7704141L (en) | HYDROFORMULATION PROCEDURE | |
ES396995A1 (en) | Method of making diffusion devices having a membrane support of photoinsolubilized plastic | |
BE811661A (en) | IGNIFUGATION OF LINEAR POLYESTERS. | |
CA1034044A (en) | Tertiary alcohol stabilized e-series prostaglandins | |
CA1007658A (en) | Superior catalyst prepared by impregnation of preformed matrix | |
FR2289511A1 (en) | Tungsten cpds. contg. silanol gps. - and tungsten complex cpds. contg. ligands used as allyl alcohol isomerisation catalysts | |
CA1011374A (en) | Fuel tank and hydraulic reservoir arrangement | |
GB1460207A (en) | Process for the preparation of 2-methylpropane-1,3-diol | |
ES204858U (en) | Headlight for vehicles. (Machine-translation by Google Translate, not legally binding) | |
ES408461A1 (en) | Motor vehicle light | |
SU523202A1 (en) | Hydraulic pressure booster | |
SU463892A1 (en) | Fluid sampler | |
SU513467A1 (en) | Control method of valve converter | |
ES429922A1 (en) | Dehydrogenation of aliphatic and cycloaliphatic alcohols | |
JPS5634651A (en) | Alpha-allyl-substituted deltaepsilon-unsaturated aldehyde | |
SU568776A1 (en) | Valve | |
AT339467B (en) | SHAPED BODIES MADE OF LIGHT STABILIZED, SYNTHETIC, LINEAR POLYESTERS | |
GB1377895A (en) | Production of ethers | |
Wilkinson | Some personality correlates of ideational persistence | |
CA1022855A (en) | Oxygenation by dialysis of h2o2 through catalyst-containing membrane |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
ST | Notification of lapse |