DE69013693T2 - Verfahren zur herstellung von dialkyl-gold(iii)-beta-diketonaten. - Google Patents
Verfahren zur herstellung von dialkyl-gold(iii)-beta-diketonaten.Info
- Publication number
- DE69013693T2 DE69013693T2 DE69013693T DE69013693T DE69013693T2 DE 69013693 T2 DE69013693 T2 DE 69013693T2 DE 69013693 T DE69013693 T DE 69013693T DE 69013693 T DE69013693 T DE 69013693T DE 69013693 T2 DE69013693 T2 DE 69013693T2
- Authority
- DE
- Germany
- Prior art keywords
- gold
- iii
- dialkyl
- diketone
- trifluoroacetylacetone
- 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.)
- Expired - Fee Related
Links
- CBMIPXHVOVTTTL-UHFFFAOYSA-N gold(3+) Chemical compound [Au+3] CBMIPXHVOVTTTL-UHFFFAOYSA-N 0.000 title claims description 5
- 238000004519 manufacturing process Methods 0.000 title description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 21
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 14
- 239000010931 gold Substances 0.000 claims description 14
- 229910052737 gold Inorganic materials 0.000 claims description 14
- SHXHPUAKLCCLDV-UHFFFAOYSA-N 1,1,1-trifluoropentane-2,4-dione Chemical compound CC(=O)CC(=O)C(F)(F)F SHXHPUAKLCCLDV-UHFFFAOYSA-N 0.000 claims description 9
- 230000015572 biosynthetic process Effects 0.000 claims description 8
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 claims description 8
- 238000003786 synthesis reaction Methods 0.000 claims description 8
- 239000011541 reaction mixture Substances 0.000 claims description 7
- 229910003767 Gold(III) bromide Inorganic materials 0.000 claims description 4
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 4
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- OVWPJGBVJCTEBJ-UHFFFAOYSA-K gold tribromide Chemical compound Br[Au](Br)Br OVWPJGBVJCTEBJ-UHFFFAOYSA-K 0.000 claims description 4
- -1 i-propyllithium Chemical compound 0.000 claims description 4
- QAMFBRUWYYMMGJ-UHFFFAOYSA-N hexafluoroacetylacetone Chemical compound FC(F)(F)C(=O)CC(=O)C(F)(F)F QAMFBRUWYYMMGJ-UHFFFAOYSA-N 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 229910003803 Gold(III) chloride Inorganic materials 0.000 claims description 2
- BLHLJVCOVBYQQS-UHFFFAOYSA-N ethyllithium Chemical compound [Li]CC BLHLJVCOVBYQQS-UHFFFAOYSA-N 0.000 claims description 2
- RJHLTVSLYWWTEF-UHFFFAOYSA-K gold trichloride Chemical compound Cl[Au](Cl)Cl RJHLTVSLYWWTEF-UHFFFAOYSA-K 0.000 claims description 2
- CCZVEWRRAVASGL-UHFFFAOYSA-N lithium;2-methanidylpropane Chemical compound [Li+].CC(C)[CH2-] CCZVEWRRAVASGL-UHFFFAOYSA-N 0.000 claims description 2
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 claims description 2
- XBEREOHJDYAKDA-UHFFFAOYSA-N lithium;propane Chemical compound [Li+].CC[CH2-] XBEREOHJDYAKDA-UHFFFAOYSA-N 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 10
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- AUFHQOUHGKXFEM-UHFFFAOYSA-N C[Au]C Chemical compound C[Au]C AUFHQOUHGKXFEM-UHFFFAOYSA-N 0.000 description 5
- 239000004065 semiconductor Substances 0.000 description 5
- 238000001465 metallisation Methods 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- DJZSKFWRKYXXMH-UHFFFAOYSA-M C[Au](C)I Chemical class C[Au](C)I DJZSKFWRKYXXMH-UHFFFAOYSA-M 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 238000004809 thin layer chromatography Methods 0.000 description 3
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- FGAMHGRHEJFBPW-UHFFFAOYSA-N C[Au+]C Chemical compound C[Au+]C FGAMHGRHEJFBPW-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000013058 crude material Substances 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- 229940014053 gold tribromide Drugs 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- VXWPONVCMVLXBW-UHFFFAOYSA-M magnesium;carbanide;iodide Chemical compound [CH3-].[Mg+2].[I-] VXWPONVCMVLXBW-UHFFFAOYSA-M 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000002343 gold Chemical class 0.000 description 1
- VGQKFNVLVSFVKF-UHFFFAOYSA-N gold(3+);pentane-2,4-dione Chemical class [Au+3].CC(=O)CC(C)=O VGQKFNVLVSFVKF-UHFFFAOYSA-N 0.000 description 1
- TYJJOEBQRJABJG-UHFFFAOYSA-K gold(3+);pyridine;trichloride Chemical compound [Cl-].[Cl-].[Cl-].[Au+3].C1=CC=NC=C1 TYJJOEBQRJABJG-UHFFFAOYSA-K 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- IHLVCKWPAMTVTG-UHFFFAOYSA-N lithium;carbanide Chemical compound [Li+].[CH3-] IHLVCKWPAMTVTG-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 150000003475 thallium Chemical class 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
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
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic Table
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/517,272 US5023360A (en) | 1990-05-01 | 1990-05-01 | Simplified synthesis of dialkylgold(III) β-diketonates |
| PCT/US1990/005899 WO1991017167A1 (en) | 1990-05-01 | 1990-10-15 | Synthesis of dialkyl gold (iii) beta-diketonates |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69013693D1 DE69013693D1 (de) | 1994-12-01 |
| DE69013693T2 true DE69013693T2 (de) | 1995-05-04 |
Family
ID=24059120
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69013693T Expired - Fee Related DE69013693T2 (de) | 1990-05-01 | 1990-10-15 | Verfahren zur herstellung von dialkyl-gold(iii)-beta-diketonaten. |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US5023360A (OSRAM) |
| EP (1) | EP0530187B1 (OSRAM) |
| JP (1) | JPH05502020A (OSRAM) |
| DE (1) | DE69013693T2 (OSRAM) |
| WO (1) | WO1991017167A1 (OSRAM) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6951868B2 (en) | 2001-11-09 | 2005-10-04 | Pfizer Inc. | Azabicyclic-phenyl-fused-heterocyclic compounds for treatment of disease |
| CN108752179A (zh) * | 2018-07-16 | 2018-11-06 | 扬州工业职业技术学院 | 一种二甲基乙酰丙酮金的制备方法及其应用 |
-
1990
- 1990-05-01 US US07/517,272 patent/US5023360A/en not_active Expired - Fee Related
- 1990-10-15 DE DE69013693T patent/DE69013693T2/de not_active Expired - Fee Related
- 1990-10-15 EP EP90916578A patent/EP0530187B1/en not_active Expired - Lifetime
- 1990-10-15 WO PCT/US1990/005899 patent/WO1991017167A1/en not_active Ceased
- 1990-10-15 JP JP2515577A patent/JPH05502020A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DE69013693D1 (de) | 1994-12-01 |
| JPH0583556B2 (OSRAM) | 1993-11-26 |
| US5023360A (en) | 1991-06-11 |
| WO1991017167A1 (en) | 1991-11-14 |
| JPH05502020A (ja) | 1993-04-15 |
| EP0530187A1 (en) | 1993-03-10 |
| EP0530187B1 (en) | 1994-10-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0398132B1 (de) | Phosphorverbindungen | |
| DE1148551B (de) | Verfahren zur Herstellung von Phosphonsaeuren bzw. deren Salzen mit mindestens 2 Phosphoratomen im Molekuel | |
| WO1993015089A1 (de) | Diphosphinliganden | |
| DE2914294C2 (de) | Verfahren zur Herstellung von Verbindungen mit Phosphor-Kohlenstoff-Stickstoff-Bindung | |
| DE3000445A1 (de) | Optisch aktive 1,2-bis-(diphenylphosphino)-verbindungen, diese als chirale liganden enthaltenden metallkomplexe und deren verwendung | |
| DE3717265A1 (de) | Verfahren zum herstellen von disilylmethanen | |
| DE2141186B2 (de) | Verfahren zur Herstellung primärer oder sekundärer, ungesättigter Cg u. Cn - Alkohole | |
| DE2502919C2 (de) | Cyclopentan-Derivate, Verfahren zu ihrer Herstellung, sowie diese enthaltende pharmazeutische Zusammensetzungen | |
| EP0530187B1 (en) | Synthesis of dialkyl gold (iii) beta-diketonates | |
| DE69001266T2 (de) | Cyclische triketonverbindungen und trimethylsilylbutadienverbindungen und ihre verwendung zur herstellung von daunomycinon-derivaten. | |
| CH624930A5 (OSRAM) | ||
| DE2350195C2 (de) | Verfahren zur Herstellung von Derivaten dimerisierter konjugierter Diene | |
| DE1816282A1 (de) | Verfahren zur Herstellung von Hydroxy- oder Mercaptogruppen enthaltenden organischen Verbindungen | |
| EP0144743B1 (de) | Verfahren zur Herstellung organischer Chlorphosphane | |
| DE2460288C3 (de) | Verfahren zur Herstellung von Tricyclohexylzinnchlorid oder -bromid | |
| DE19809341C1 (de) | Verfahren zur selektiven Alkylierung von Aldehyden mit Organozinkverbindungen | |
| DE2365322C3 (de) | Subst.-Methyl-phosphonsäuredimethylester und ein Verfahren zu ihrer Herstellung | |
| DE1568863C (de) | Verschiedene Übergangsmetallatome enthaltende zweikernige Brückenkomplexverbindungen | |
| DE3323392A1 (de) | Verfahren zur herstellung von derivaten der vinylphosphon-, oder vinylpyrophosphonsaeure | |
| DE1793694C3 (de) | Helveticosidderivate | |
| DE2033360C3 (de) | 23,43-Tetrastearoylhexanhexitol-(l,6)-di-(phosphorsäurecholinester) und Verfahren zu deren Herstellung | |
| DE1793685C3 (de) | Helveticosidderivate | |
| DE3636963A1 (de) | Neue trimethylsilyl-carbamate und verfahren zu ihrer herstellung | |
| DE889746C (de) | Verfahren zur Darstellung von androgen hochwirksamen 17-Derivaten von Androstanoxyketonen | |
| DE3942789A1 (de) | Sulfoniertes triphenylphosphan enthaltende komplexverbindung des rhodiums |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |